62830-55-1|(4-Iodophenyl)hydrazine hydrochloride| Ambeed

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Quality Control of [ 62830-55-1 ] Purity: 97% SDS Specification

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Product Details of [ 62830-55-1 ]

CAS No. :	62830-55-1
Formula :	C₆H₈ClIN₂
M.W :	270.50
SMILES Code :	NNC1=CC=C(I)C=C1.[H]Cl
MDL No. :	MFCD00060724
InChI Key :	PBGQZFXOUDOZCB-UHFFFAOYSA-N
Pubchem ID :	12208795

Safety of [ 62830-55-1 ]

GHS Pictogram:
Signal Word:	Warning
Hazard Statements:	H302-H315-H319-H335
Precautionary Statements:	P280-P305+P351+P338

Computational Chemistry of [ 62830-55-1 ] Show Less

Physicochemical Properties

Num. heavy atoms	10
Num. arom. heavy atoms	6
Fraction Csp3	0.0
Num. rotatable bonds	1
Num. H-bond acceptors	1.0
Num. H-bond donors	2.0
Molar Refractivity	53.33
TPSA ? Topological Polar Surface Area: Calculated from Ertl P. et al. 2000 J. Med. Chem.	38.05 Å²

Lipophilicity

Log P_o/w (iLOGP)? iLOGP: in-house physics-based method implemented from Daina A et al. 2014 J. Chem. Inf. Model.	0.0
Log P_o/w (XLOGP3)? XLOGP3: Atomistic and knowledge-based method calculated by XLOGP program, version 3.2.2, courtesy of CCBG, Shanghai Institute of Organic Chemistry	3.06
Log P_o/w (WLOGP)? WLOGP: Atomistic method implemented from Wildman SA and Crippen GM. 1999 J. Chem. Inf. Model.	2.19
Log P_o/w (MLOGP)? MLOGP: Topological method implemented from Moriguchi I. et al. 1992 Chem. Pharm. Bull. Moriguchi I. et al. 1994 Chem. Pharm. Bull. Lipinski PA. et al. 2001 Adv. Drug. Deliv. Rev.	2.61
Log P_o/w (SILICOS-IT)? SILICOS-IT: Hybrid fragmental/topological method calculated by FILTER-IT program, version 1.0.2, courtesy of SILICOS-IT, http://www.silicos-it.com	1.33
Consensus Log P_o/w? Consensus Log P_o/w: Average of all five predictions	1.84

Water Solubility

Log S (ESOL):? ESOL: Topological method implemented from Delaney JS. 2004 J. Chem. Inf. Model.	-3.82
Solubility	0.0407 mg/ml ; 0.00015 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Soluble
Log S (Ali)? Ali: Topological method implemented from Ali J. et al. 2012 J. Chem. Inf. Model.	-3.53
Solubility	0.0806 mg/ml ; 0.000298 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Soluble
Log S (SILICOS-IT)? SILICOS-IT: Fragmental method calculated by FILTER-IT program, version 1.0.2, courtesy of SILICOS-IT, http://www.silicos-it.com	-3.05
Solubility	0.243 mg/ml ; 0.000897 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Soluble

Pharmacokinetics

GI absorption? Gatrointestinal absorption: according to the white of the BOILED-Egg	High
BBB permeant? BBB permeation: according to the yolk of the BOILED-Egg	Yes
P-gp substrate? P-glycoprotein substrate: SVM model built on 1033 molecules (training set) and tested on 415 molecules (test set) 10-fold CV: ACC=0.72 / AUC=0.77 External: ACC=0.88 / AUC=0.94	No
CYP1A2 inhibitor? Cytochrome P450 1A2 inhibitor: SVM model built on 9145 molecules (training set) and tested on 3000 molecules (test set) 10-fold CV: ACC=0.83 / AUC=0.90 External: ACC=0.84 / AUC=0.91	No
CYP2C19 inhibitor? Cytochrome P450 2C19 inhibitor: SVM model built on 9272 molecules (training set) and tested on 3000 molecules (test set) 10-fold CV: ACC=0.80 / AUC=0.86 External: ACC=0.80 / AUC=0.87	No
CYP2C9 inhibitor? Cytochrome P450 2C9 inhibitor: SVM model built on 5940 molecules (training set) and tested on 2075 molecules (test set) 10-fold CV: ACC=0.78 / AUC=0.85 External: ACC=0.71 / AUC=0.81	No
CYP2D6 inhibitor? Cytochrome P450 2D6 inhibitor: SVM model built on 3664 molecules (training set) and tested on 1068 molecules (test set) 10-fold CV: ACC=0.79 / AUC=0.85 External: ACC=0.81 / AUC=0.87	No
CYP3A4 inhibitor? Cytochrome P450 3A4 inhibitor: SVM model built on 7518 molecules (training set) and tested on 2579 molecules (test set) 10-fold CV: ACC=0.77 / AUC=0.85 External: ACC=0.78 / AUC=0.86	No
Log Kp (skin permeation)? Skin permeation: QSPR model implemented from Potts RO and Guy RH. 1992 Pharm. Res.	-5.78 cm/s

Druglikeness

Lipinski? Lipinski (Pfizer) filter: implemented from Lipinski CA. et al. 2001 Adv. Drug Deliv. Rev. MW ≤ 500 MLOGP ≤ 4.15 N or O ≤ 10 NH or OH ≤ 5	0.0
Ghose? Ghose filter: implemented from Ghose AK. et al. 1999 J. Comb. Chem. 160 ≤ MW ≤ 480 -0.4 ≤ WLOGP ≤ 5.6 40 ≤ MR ≤ 130 20 ≤ atoms ≤ 70	None
Veber? Veber (GSK) filter: implemented from Veber DF. et al. 2002 J. Med. Chem. Rotatable bonds ≤ 10 TPSA ≤ 140	0.0
Egan? Egan (Pharmacia) filter: implemented from Egan WJ. et al. 2000 J. Med. Chem. WLOGP ≤ 5.88 TPSA ≤ 131.6	0.0
Muegge? Muegge (Bayer) filter: implemented from Muegge I. et al. 2001 J. Med. Chem. 200 ≤ MW ≤ 600 -2 ≤ XLOGP ≤ 5 TPSA ≤ 150 Num. rings ≤ 7 Num. carbon > 4 Num. heteroatoms > 1 Num. rotatable bonds ≤ 15 H-bond acc. ≤ 10 H-bond don. ≤ 5	0.0
Bioavailability Score? Abbott Bioavailability Score: Probability of F > 10% in rat implemented from Martin YC. 2005 J. Med. Chem.	0.55

Medicinal Chemistry

PAINS? Pan Assay Interference Structures: implemented from Baell JB. & Holloway GA. 2010 J. Med. Chem.	0.0 alert
Brenk? Structural Alert: implemented from Brenk R. et al. 2008 ChemMedChem	2.0 alert: heavy_metal
Leadlikeness? Leadlikeness: implemented from Teague SJ. 1999 Angew. Chem. Int. Ed. 250 ≤ MW ≤ 350 XLOGP ≤ 3.5 Num. rotatable bonds ≤ 7	No; 1 violation:MW<0.0
Synthetic accessibility? Synthetic accessibility score: from 1 (very easy) to 10 (very difficult) based on 1024 fragmental contributions (FP2) modulated by size and complexity penaties, trained on 12'782'590 molecules and tested on 40 external molecules (r² = 0.94)	2.23

Application In Synthesis of [ 62830-55-1 ]

* 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.

Downstream synthetic route of [ 62830-55-1 ]

[ 62830-55-1 ] Synthesis Path-Downstream 1~35

1
[ 113313-18-1 ]
[ 62830-55-1 ]
[ 130180-11-9 ]

References: [1]Archiv der Pharmazie,1990,vol. 323,p. 471 - 474.

2
[ 130117-35-0 ]
[ 62830-55-1 ]
[ 130180-03-9 ]

References: [1]Archiv der Pharmazie,1990,vol. 323,p. 471 - 474.

3
[ 72775-93-0 ]
[ 62830-55-1 ]
[ 130180-18-6 ]

References: [1]Archiv der Pharmazie,1990,vol. 323,p. 471 - 474.

4
[ 72775-93-0 ]
[ 62830-55-1 ]
[ 130179-96-3 ]

References: [1]Archiv der Pharmazie,1990,vol. 323,p. 471 - 474.

5
[ 483-55-6 ]
[ 62830-55-1 ]
[ 62830-27-7 ]

References: [1]Pharmazie,1976,vol. 31,p. 856 - 859.

6
[ 29366-46-9 ]
[ 62830-55-1 ]
[ 62830-29-9 ]

References: [1]Pharmazie,1976,vol. 31,p. 856 - 859.

7
[ 29366-44-7 ]
[ 62830-55-1 ]
[ 62830-28-8 ]

References: [1]Pharmazie,1976,vol. 31,p. 856 - 859.

8
[ 62830-54-0 ]
[ 62830-55-1 ]
[ 62830-31-3 ]

References: [1]Pharmazie,1976,vol. 31,p. 856 - 859.

9
[ 62830-53-9 ]
[ 62830-55-1 ]
[ 62830-30-2 ]

References: [1]Pharmazie,1976,vol. 31,p. 856 - 859.

10
[ 62830-55-1 ]
Methyl 2-(dimethoxyphosphonyl)-3-hydroxy-2-propenoate sodium salt [ No CAS ]
Dimethyl [1-(4-iodoophenyl)-5-hydroxy-1H-pyrazol-4-yl]phosphonate [ No CAS ]

References: [1]Organic Preparations and Procedures International,1999,vol. 31,p. 295 - 304.

11
[ 62830-55-1 ]
[ 823821-72-3 ]
<i>N</i>-[3-(5-iodo-3-phenyl-1<i>H</i>-indol-2-yl)-propyl]-acetamide [ No CAS ]

References: [1]Mendeleev Communications,2006,vol. 16,p. 213 - 215.

12
[ 13436-46-9 ]
[ 62830-55-1 ]
[ 936252-57-2 ]

References: [1]Journal of Medicinal Chemistry,2007,vol. 50,p. 1810 - 1827.

13
[ 62830-55-1 ]
2-(3"-(5"-iodo-indolyl)ethyloxy)adenosine [ No CAS ]

References: [1]Journal of Medicinal Chemistry,2007,vol. 50,p. 1810 - 1827.

14
[ 62830-55-1 ]
[ 936252-64-1 ]

References: [1]Journal of Medicinal Chemistry,2007,vol. 50,p. 1810 - 1827.

15
[ 62830-55-1 ]
[ 936252-82-3 ]

References: [1]Journal of Medicinal Chemistry,2007,vol. 50,p. 1810 - 1827.

16
[ 62830-55-1 ]
[ 936252-96-9 ]

References: [1]Journal of Medicinal Chemistry,2007,vol. 50,p. 1810 - 1827.

17
[ 56461-20-2 ]
[ 62830-55-1 ]
8-Iodo-5,10-dihydro-indeno[1,2-b]indole-1-carboxylic acid [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
5%	With hydrogenchloride; In formic acid;	EXAMPLE 17 8-Iodo-5,10-dihydro-indeno[1,2-b]indole-1-carboxylic acid 0.6 hydrate 1-Oxo-indan4-carboxylic acid (0.528 g, 2.99 mmol) and <strong>[62830-55-1]4-iodophenylhydrazine hydrochloride</strong> (0.698 g, 2.58 mmol) were mixed together in a Teflon PFA vessel to form a paste in formic acid (2 mL, 96percent) containing 3 drops of concentrated HCl. The vessel was irradiated at full power (760 W) in a CEM Microwave (MDS2000) for one minute (T=140 C, P<50 PSI), allowed to cool for 2 min, then irradiated again for one min (T=140 C, P<50 PSI). The mixture was vacuum filtered hot. The solid was washed with formic acid, and dried on the frit. Chromatography (acetone/hexane) and trituration with diethyl ether gave the title compound (0.059 g, 5percent) as an tan solid: mp 251° C.; 1H NMR (DMSO-d6): delta 3.98 (s, 2H), 7.30-7.37 (m, 2H), 7.49 (t, 1H), 7.77-7.80 (m, 2H), 7.98 (d, 1H), 11.82 (s, 1H), 13.53 (s, 1H); MS [EI, m/z]: 375 [M]+. Elemental analysis for C16H10INO2.0.6(H2O)Calc'd: C, 49.87; H, 2.72; N, 3.63Found: C, 49.59; H, 2.81; N, 3.66

References: [1]Patent: US6288099,2001,B1 .

18
[ 1445-73-4 ]
[ 62830-55-1 ]
[ 1147939-50-1 ]

Yield	Reaction Conditions	Operation in experiment
		To a suspension of <strong>[62830-55-1]4-iodophenylhydrazine hydrochloride</strong> (2.0 g, 0.0074 mol) in dioxane (30 mL) at RT was added cone. H2SO4 (0.7 mL, 0.0171 mol) dropwise and the reaction mixture was stirred for 5 min. To this was added N-methyl-4-piperidone (0.838 g, 0.0074 mol) and the reaction mixture was stirred at RT for 10 min and heated at 70 0C for 90 min. Reaction monitored by TLC. The solvent was evaporated and pH adjusted to 9-10 by 10percent KOH Solution. The product was extracted with (3x50 rnL) EtOAc. Combined organic layer washed with water and brine and dried over sodium sulfate, concentrated under vacuum and product purified by column chromatography (100-200 mesh silica) in solvent system (0-10percent, DCM/MeOH). Obtained 1.8g of brown solid. 1U NMR (CDCl3, free base) d (ppm) 7.70 (s, IH), 7.38 (d, IH), 7.05 (d, IH), 3.60 (s, 2H), 2.90 (m, 4H), 2.58 (s, 3H).

References: [1]Patent: WO2010/51501,2010,A1 .Location in patent: Page/Page column 242-243.

19
[ 62830-55-1 ]
[ 372-31-6 ]
[ 1257412-06-8 ]