[ CAS No. 12080-32-9 ] {[proInfo.proName]}

Name: 12080-32-9|Dichloro(1,5-cyclooctadiene)platinum(II)|98%
Brand: Ambeed
SKU: A381753
Price: 12.0 USD
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2D 3D

Structure of 12080-32-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 12080-32-9 ]

COA NMR CNMR HPLC LC-MS

Related Doc. of [ 12080-32-9 ]

SDS Specification

Alternatived Products of [ 12080-32-9 ]

Product Details of [ 12080-32-9 ]

CAS No. :	12080-32-9	MDL No. :	MFCD00012413
Formula :	C₈H₁₂Cl₂Pt	Boiling Point :	-
Linear Structure Formula :	-	InChI Key :	-
M.W :	374.17	Pubchem ID :	-
Synonyms :

Calculated chemistry of [ 12080-32-9 ]

Physicochemical Properties

Num. heavy atoms :	11
Num. arom. heavy atoms :	0
Fraction Csp3 :	0.5
Num. rotatable bonds :	0
Num. H-bond acceptors :	0.0
Num. H-bond donors :	0.0
Molar Refractivity :	49.21
TPSA :	0.0 Å²

Pharmacokinetics

GI absorption :	Low
BBB permeant :	No
P-gp substrate :	No
CYP1A2 inhibitor :	No
CYP2C19 inhibitor :	No
CYP2C9 inhibitor :	No
CYP2D6 inhibitor :	No
CYP3A4 inhibitor :	No
Log Kp (skin permeation) :	-5.2 cm/s

Lipophilicity

Log Po/w (iLOGP) :	0.0
Log Po/w (XLOGP3) :	4.76
Log Po/w (WLOGP) :	-3.32
Log Po/w (MLOGP) :	3.27
Log Po/w (SILICOS-IT) :	2.28
Consensus Log Po/w :	1.4

Druglikeness

Lipinski :	0.0
Ghose :	None
Veber :	0.0
Egan :	0.0
Muegge :	1.0
Bioavailability Score :	0.55

Water Solubility

Log S (ESOL) :	-5.16
Solubility :	0.0026 mg/ml ; 0.00000694 mol/l
Class :	Moderately soluble
Log S (Ali) :	-4.49
Solubility :	0.0121 mg/ml ; 0.0000323 mol/l
Class :	Moderately soluble
Log S (SILICOS-IT) :	-1.1
Solubility :	29.5 mg/ml ; 0.0789 mol/l
Class :	Soluble

Medicinal Chemistry

PAINS :	0.0 alert
Brenk :	1.0 alert
Leadlikeness :	2.0
Synthetic accessibility :	2.88

Safety of [ 12080-32-9 ]

Signal Word:	Warning	Class:	N/A
Precautionary Statements:	P261-P305+P351+P338	UN#:	N/A
Hazard Statements:	H315-H319-H335	Packing Group:	N/A
GHS Pictogram:

Application In Synthesis of [ 12080-32-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

Upstream synthesis route of [ 12080-32-9 ]
Downstream synthetic route of [ 12080-32-9 ]

[ 12080-32-9 ] Synthesis Path-Upstream 1~15

1
[ 10025-99-7 ]
[ 5259-72-3 ]
[ 12080-32-9 ]

Yield	Reaction Conditions	Operation in experiment
80%	With acetic acid In water at 90℃; for 0.5 h; Darkness	2.1.4.1 Synthesis of cis-dichlorido(1.5-cyclooctadiene)platinum(II), [Pt(cod)Cl₂] (0014) K₂PtCl₄ (1.000g, 2.4mmol) was dissolved in water (16mL) and the resulting solution was filtered. To the filtered deep red solution, acetic acid (24mL) and 1,5-cyclooctadiene (cod) (1.00mL, 8.1mmol) were added, in the dark. The reaction mixture was stirred and heated at ca. 90°C in a water bath. Over 30min the deep red solution slowly became pale yellow and some precipitation was observed. After ca. 2h, the volume of the solution was reduced to 10mL by evaporation under reduced pressure. The obtained precipitate was then centrifuged and washed with water, ethanol and diethyl ether. Yield: 703mg (80percent). ¹H NMR (CDCl₃-d₃) δ: 5.60 (4H, t, CH), 2.70 (2H, m, CH₂−CH), 2.30–2.16 (2H, m, CH₂−CH) ppm; ¹³C{¹H} NMR (CDCl₃-d₃) δ: 100.0 (CH), 30.0 (CH₂) ppm; ¹⁹⁵Pt NMR (CDCl₃-d₃) δ: −3340ppm.

Reference： [1] Chemistry - An Asian Journal, 2018, vol. 13, # 8, p. 1053 - 1059
[2] Dalton Transactions, 2008, # 47, p. 6724 - 6731
[3] Organometallics, 2014, vol. 33, # 15, p. 4027 - 4034
[4] Journal of the American Chemical Society, 2015, vol. 137, # 42, p. 13464 - 13467
[5] Journal of Inorganic Biochemistry, 2016, vol. 160, p. 275 - 286
[6] Journal of Organometallic Chemistry, 2006, vol. 691, # 26, p. 5845 - 5855
[7] Dalton Transactions, 2017, vol. 46, # 31, p. 10246 - 10254
[8] Organometallics, 2005, vol. 24, # 21, p. 5038 - 5043

2
[ 5259-72-3 ]
[ 12080-32-9 ]

Reference： [1] Journal of Organometallic Chemistry, 2011, vol. 696, # 7, p. 1349 - 1354
[2] Journal of Organometallic Chemistry, 2011, vol. 696, # 7, p. 1349 - 1354

3
[ 75-09-2 ]
[ 608134-69-6 ]
[ 56-34-8 ]
[ 12080-32-9 ]

Reference： [1] Organometallics, 2008, vol. 27, # 6, p. 1234 - 1241

4
[ 143168-86-9 ]
[ 5259-72-3 ]
[ 12080-32-9 ]

Reference： [1] Russian Journal of General Chemistry, 2005, vol. 75, # 3, p. 321 - 324

5
[ 608134-69-6 ]
[ 115-11-7 ]
[ 12080-32-9 ]
[ 62904-80-7 ]

Reference： [1] Organometallics, 2009, vol. 28, # 24, p. 6935 - 6943
[2] Organometallics, 2009, vol. 28, # 24, p. 6935 - 6943

6
[ 12266-72-7 ]
[ 98-80-6 ]
[ 12080-32-9 ]

Reference： [1] Organometallics, 2006, vol. 25, # 13, p. 3251 - 3258

7
[ 25478-60-8 ]
[ 5259-72-3 ]
[ 12080-32-9 ]

Reference： [1] Organometallics, 2005, vol. 24, # 18, p. 4427 - 4431
[2] Organometallics, 2005, vol. 24, # 18, p. 4427 - 4431

8
[ 5259-72-3 ]
[ 12080-32-9 ]

Reference： [1] Organometallics, 2006, vol. 25, # 3, p. 678 - 683

9
[ 608134-68-5 ]
[ 201230-82-2 ]
[ 12080-32-9 ]

Reference： [1] Organometallics, 2008, vol. 27, # 18, p. 4810 - 4816

10
[ 498-66-8 ]
[ 608134-69-6 ]
[ 12080-32-9 ]
[ 57158-98-2 ]

Reference： [1] Organometallics, 2009, vol. 28, # 24, p. 6935 - 6943

11
[ 12107-56-1 ]
[ 12080-32-9 ]
[ 53761-88-9 ]

Reference： [1] Bulletin of the Chemical Society of Japan, 2004, vol. 77, # 1, p. 139 - 145

12
[ 12107-56-1 ]
[ 12080-32-9 ]
[ 53761-88-9 ]

Reference： [1] Bulletin of the Chemical Society of Japan, 2004, vol. 77, # 1, p. 139 - 145

13
[ 10025-99-7 ]
[ 1552-12-1 ]
[ 12080-32-9 ]

Reference： [1] Polyhedron, 2013, vol. 50, # 1, p. 82 - 89

14
[ 5259-72-3 ]
[ 12080-32-9 ]

Reference： [1] Russian Journal of General Chemistry, 2000, vol. 70, # 8, p. 1240 - 1242

15
[ 14104-20-2 ]
[ 12107-56-1 ]
[ 67-64-1 ]
[ 7647-14-5 ]
[ 12080-32-9 ]
[ 53761-88-9 ]

Reference： [1] Bulletin of the Chemical Society of Japan, 2004, vol. 77, # 1, p. 139 - 145

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Yield	Reaction Conditions	Operation in experiment
90%	In dichloromethane; for 0.166667h;	b) cis-[PtCl2(PPh3)2] A solution of 2.6 g (7 mmoles) of cis-[PtCl2(1,5-cyclooctadiene)] in 80 ml of CH2Cl2 is added, drop by drop, with a solution of 3.7 g (14 mmoles) of PPh3 dissolved in 100 ml of CH2Cl2. Ten minutes after the end of the addition, the solvent is evaporated off under reduced pressure, the residue is washed with n-hexane and filtered through a porous septum. 5 g (6.3 mmoles) of product as a white solid are obtained (yield: 90%).
	In dichloromethane;	The complex cis-[PtCl2(PPh3)2] was prepared by reaction of [PtCl2(cod)] (cod=1,5-cyclooctadiene) [34] with 2mol equivalents of PPh3 in dichloromethane, followed by precipitation of the product with petroleum spirits

Yield	Reaction Conditions	Operation in experiment
59%	With KOH; CH₂Cl₂ In tetrahydrofuran; dichloromethane addn. of phosphine, sulfamide and KOH (excess) to a stirred Pt complex suspension under N2; refluxing, 1.5 h; filtration; evapn. to dryness; dissolving in CH2Cl2; washing (H2O); separation of organic layer; drying (MgSO4); evapn.; addn. of Et2O; pptn.; filtration; drying (vac.); identification by NMR;
15%	With Ag₂O; CH₂Cl₂ In dichloromethane addn. of phosphine, then of diphenylsulfamide and Ag2O (excess) to a stirred Pt complex soln. under N2; refluxing, 3 h; filtration; evapn. to dryness; dissolving in CH2Cl2; addn. of light petroleum; pptn.; recrystn. (CH2Cl2/light petroleum); drying (vac.); elem. anal.;

Physical hazards
Code	Phrase
H200	Unstable explosive
H201	Explosive; mass explosion hazard
H202	Explosive; severe projection hazard
H203	Explosive; fire, blast or projection hazard
H204	Fire or projection hazard
H205	May mass explode in fire
H220	Extremely flammable gas
H221	Flammable gas
H222	Extremely flammable aerosol
H223	Flammable aerosol
H224	Extremely flammable liquid and vapour
H225	Highly flammable liquid and vapour
H226	Flammable liquid and vapour
H227	Combustible liquid
H228	Flammable solid
H229	Pressurized container: may burst if heated
H230	May react explosively even in the absence of air
H231	May react explosively even in the absence of air at elevated pressure and/or temperature
H240	Heating may cause an explosion
H241	Heating may cause a fire or explosion
H242	Heating may cause a fire
H250	Catches fire spontaneously if exposed to air
H251	Self-heating; may catch fire
H252	Self-heating in large quantities; may catch fire
H260	In contact with water releases flammable gases which may ignite spontaneously
H261	In contact with water releases flammable gas
H270	May cause or intensify fire; oxidizer
H271	May cause fire or explosion; strong oxidizer
H272	May intensify fire; oxidizer
H280	Contains gas under pressure; may explode if heated
H281	Contains refrigerated gas; may cause cryogenic burns or injury
H290	May be corrosive to metals
Health hazards
Code	Phrase
H300	Fatal if swallowed
H301	Toxic if swallowed
H302	Harmful if swallowed
H303	May be harmful if swallowed
H304	May be fatal if swallowed and enters airways
H305	May be harmful if swallowed and enters airways
H310	Fatal in contact with skin
H311	Toxic in contact with skin
H312	Harmful in contact with skin
H313	May be harmful in contact with skin
H314	Causes severe skin burns and eye damage
H315	Causes skin irritation
H316	Causes mild skin irritation
H317	May cause an allergic skin reaction
H318	Causes serious eye damage
H319	Causes serious eye irritation
H320	Causes eye irritation
H330	Fatal if inhaled
H331	Toxic if inhaled
H332	Harmful if inhaled
H333	May be harmful if inhaled
H334	May cause allergy or asthma symptoms or breathing difficulties if inhaled
H335	May cause respiratory irritation
H336	May cause drowsiness or dizziness
H340	May cause genetic defects
H341	Suspected of causing genetic defects
H350	May cause cancer
H351	Suspected of causing cancer
H360	May damage fertility or the unborn child
H361	Suspected of damaging fertility or the unborn child
H361d	Suspected of damaging the unborn child
H362	May cause harm to breast-fed children
H370	Causes damage to organs
H371	May cause damage to organs
H372	Causes damage to organs through prolonged or repeated exposure
H373	May cause damage to organs through prolonged or repeated exposure
Environmental hazards
Code	Phrase
H400	Very toxic to aquatic life
H401	Toxic to aquatic life
H402	Harmful to aquatic life
H410	Very toxic to aquatic life with long-lasting effects
H411	Toxic to aquatic life with long-lasting effects
H412	Harmful to aquatic life with long-lasting effects
H413	May cause long-lasting harmful effects to aquatic life
H420	Harms public health and the environment by destroying ozone in the upper atmosphere

Yield	Reaction Conditions	Operation in experiment
88%	With pentane In toluene (Ar), addition (pentane); washing (pentane);
	In not given

Yield	Reaction Conditions	Operation in experiment
85%	In chloroform Pt-compd. addn. to stirred soln. of org. compd. over 45 min, soln. stirring 1 h, concn. to half of vol., crystn. on Et2O slow addn.; crystals filtration, washing (ether); elem. anal.;
	In dichloromethane-d2 (under Ar, Schlenk); ligand and Pt-complex dissolved in CD2Cl2, stirred for 30 min at room temp.; monitored by NMR;

[ CAS No. 12080-32-9 ] {[proInfo.proName]}

Quality Control of [ 12080-32-9 ]

Related Doc. of [ 12080-32-9 ]

Product Details of [ 12080-32-9 ]

Calculated chemistry of [ 12080-32-9 ]

Physicochemical Properties

Pharmacokinetics

Lipophilicity

Druglikeness

Water Solubility

Medicinal Chemistry

Safety of [ 12080-32-9 ]

Application In Synthesis of [ 12080-32-9 ]

[ 12080-32-9 ] Synthesis Path-Upstream 1~15

[ 12080-32-9 ] Synthesis Path-Downstream 1~88

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

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