7343-34-2|3,5-Dimethyl-4H-1,2,4-triazole| Ambeed

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Quality Control of [ 7343-34-2 ] Purity: 97% SDS Specification

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Product Details of [ 7343-34-2 ]

CAS No. :	7343-34-2
Formula :	C₄H₇N₃
M.W :	97.12
SMILES Code :	CC1=NN=C(C)N1
MDL No. :	MFCD00656686
InChI Key :	XYYXDARQOHWBPO-UHFFFAOYSA-N
Pubchem ID :	139001

Safety of [ 7343-34-2 ]

GHS Pictogram:
Signal Word:	Warning
Hazard Statements:	H302-H315-H319-H332-H335
Precautionary Statements:	P261-P280-P305+P351+P338

Computational Chemistry of [ 7343-34-2 ] Show Less

Physicochemical Properties

Num. heavy atoms	7
Num. arom. heavy atoms	5
Fraction Csp3	0.5
Num. rotatable bonds	0
Num. H-bond acceptors	2.0
Num. H-bond donors	1.0
Molar Refractivity	26.31
TPSA ? Topological Polar Surface Area: Calculated from Ertl P. et al. 2000 J. Med. Chem.	41.57 Å²

Lipophilicity

Log P_o/w (iLOGP)? iLOGP: in-house physics-based method implemented from Daina A et al. 2014 J. Chem. Inf. Model.	0.6
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	0.27
Log P_o/w (WLOGP)? WLOGP: Atomistic method implemented from Wildman SA and Crippen GM. 1999 J. Chem. Inf. Model.	0.42
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.	-0.13
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	1.46
Consensus Log P_o/w? Consensus Log P_o/w: Average of all five predictions	0.52

Water Solubility

Log S (ESOL):? ESOL: Topological method implemented from Delaney JS. 2004 J. Chem. Inf. Model.	-1.14
Solubility	7.02 mg/ml ; 0.0723 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Very soluble
Log S (Ali)? Ali: Topological method implemented from Ali J. et al. 2012 J. Chem. Inf. Model.	-0.7
Solubility	19.2 mg/ml ; 0.198 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Very 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	-1.55
Solubility	2.72 mg/ml ; 0.028 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.	-6.7 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	2.0
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	0.0 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<1.0
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)	1.49

Application In Synthesis of [ 7343-34-2 ]

* 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 [ 7343-34-2 ]

[ 7343-34-2 ] Synthesis Path-Downstream 1~41

1
[ 1117-96-0 ]
[ 7343-34-2 ]
[ 32675-46-0 ]

References: [1]Journal of the Chemical Society,1954,p. 141,142.

2
[ 625-77-4 ]
[ 563-41-7 ]
[ 7343-34-2 ]

References: [1]Monatshefte fur Chemie,1915,vol. 36,p. 530.

3
[ 625-77-4 ]
[ 7343-34-2 ]

References: [1]Monatshefte fur Chemie,1915,vol. 36,p. 530.

4
[ 14694-34-9 ]
[ 7343-34-2 ]

References: [1]Zhurnal Obshchei Khimii,1959,vol. 29,p. 2139,2141,2142;engl.Ausg.S.2105,2107,2108.

5
[ 3069-07-6 ]
[ 7343-34-2 ]

References: [1]Chemische Berichte,1899,vol. 32,p. 797.
Journal fuer Praktische Chemie (Leipzig),1904,vol. <2> 69,p. 150.

6
[ 7343-34-2 ]
[ 471-25-0 ]
[ 156969-35-6 ]

References: [1]Australian Journal of Chemistry,1994,vol. 47,p. 991 - 1008.

7
[ 62-55-5 ]
[ 1068-57-1 ]
[ 7343-34-2 ]

References: [1]Collection of Czechoslovak Chemical Communications,1984,vol. 49,p. 2492 - 2495.

8
[ 7343-34-2 ]
[ 112-29-8 ]
[ 159255-04-6 ]

Yield	Reaction Conditions	Operation in experiment
22%	With sodium hydroxide; In N-methyl-acetamide; water;	(c) Preparation of 1-decyl-<strong>[7343-34-2]3,5-dimethyl-1,2,4-triazole</strong> A mixture of <strong>[7343-34-2]3,5-dimethyl-1,2,4-triazole</strong> (6.0 parts; 0.062 mol ex (b) above) and 1-bromodecane (14.4 parts; 0.065 mol) in dimethylformamide (16 ml) was heated together at 120° C. for 23 hours. The cooled reaction mixture was diluted with water (100 ml), a solution of sodium hydroxide (2.62 parts; 0.065 mol) in water (100 ml) added, and the product extracted into ether (3*50 ml). After drying over magnesium sulphate the solution was evaporated to yield a pale yellow oil (3.3 parts; 22percent theory). Infra red analysis: vmax (film): 2923, 2853, 1515, 1341, 701cm-1. Proton NMR: delta(CDCl3; 0.9(t,3H); 1.2-1.4(m,14H); 1.7-1.9(m,2H); 2.3(s,3H); 2.4(s,3H); 4.0(t,2H)ppm. Mass spec: m/z(Br): 238(M+H+, 100percent).

References: [1]Patent: US5620595,1997,A .

9
[ 7343-34-2 ]
2Cu⁽¹⁺⁾*(C₄H₂S(CHNCH₂)(CHNCH₂C(CH₃)2))2*2CH₃CN*2ClO₄^(1-) = [Cu₂(C₄H₂S(CHNCH₂)(CHNCH₂C(CH₃)2))2(CH₃CN)2][ClO₄]2 [ No CAS ]
silver perchlorate [ No CAS ]
Cu₄Ag((C₄H₂S(CHNCH₂)(CHNCH₂C(CH₃)2))2)2(C₄N₃H₆)2⁽³⁺⁾*3ClO₄^(1-) = [Cu₄Ag((C₄H₂S(CHNCH₂)2(C(CH₃)2))2)2(C₄N₃H₆)2][ClO₄]3 [ No CAS ]

References: [1]Journal of the Chemical Society. Chemical communications,1985,p. 262 - 263.

10
[ 7343-34-2 ]
Cu₂(C₄H₂O(CHNCH₂)(CHNCH₂C(CH₃)2))2(CH₃CN)2⁽²⁺⁾*2ClO₄^(1-) = [Cu₂(C₄H₂O(CHNCH₂)(CHNCH₂C(CH₃)2))2(CH₃CN)2][ClO₄]2 [ No CAS ]
silver perchlorate [ No CAS ]
Cu₄Ag((C₄H₂O(CHNCH₂)(CHNCH₂C(CH₃)2))2)2(C₄N₃H₆)2⁽³⁺⁾*3ClO₄^(1-) = [Cu₄Ag((C₄H₂O(CHNCH₂)2(C(CH₃)2))2)2(C₄N₃H₆)2][ClO₄]3 [ No CAS ]

References: [1]Journal of the Chemical Society. Chemical communications,1985,p. 262 - 263.

11
[ 7343-34-2 ]
Cu₂(C₄H₂O(CHNCH₂)(CHNCH₂C(CH₃)2))2(CH₃CN)2⁽²⁺⁾*2ClO₄^(1-) = [Cu₂(C₄H₂O(CHNCH₂)(CHNCH₂C(CH₃)2))2(CH₃CN)2][ClO₄]2 [ No CAS ]
[ 14057-91-1 ]
Cu₅((C₄H₂O(CHNCH₂)(CHNCH₂C(CH₃)2))2)2(C₄N₃H₆)2⁽³⁺⁾*3ClO₄^(1-) = [Cu₅((C₄H₂O(CHNCH₂)(CHNCH₂C(CH₃)2))2)2(C₄N₃H₆)2][ClO₄]3 [ No CAS ]

References: [1]Journal of the Chemical Society. Chemical communications,1985,p. 262 - 263.

12
[ 7343-34-2 ]
2Cu⁽¹⁺⁾*(C₄H₂S(CHNCH₂)(CHNCH₂C(CH₃)2))2*2CH₃CN*2ClO₄^(1-) = [Cu₂(C₄H₂S(CHNCH₂)(CHNCH₂C(CH₃)2))2(CH₃CN)2][ClO₄]2 [ No CAS ]
[ 14057-91-1 ]
Cu₅((C₄H₂S(CHNCH₂)(CHNCH₂C(CH₃)2))2)2(C₄N₃H₆)2⁽³⁺⁾*3ClO₄^(1-) = [Cu₅((C₄H₂S(CHNCH₂)(CHNCH₂C(CH₃)2))2)2(C₄N₃H₆)2][ClO₄]3 [ No CAS ]

References: [1]Journal of the Chemical Society. Chemical communications,1985,p. 262 - 263.

13
[ 7343-34-2 ]
[ 14057-91-1 ]
[Cu₂(C₄H₂O(CHNCH₂)(CHNCH₂CH₂))2(CH₃CN)2]⁽²⁺⁾*2ClO₄^(1-) = [Cu₂(C₄H₂O(CHNCH₂)(CHNCH₂CH₂))2(CH₃CN)2](ClO₄)2 [ No CAS ]
Cu₅((C₄H₂O(CHNCH₂)(CHNCH₂CH₂))2)2(C₂N₃(CH₃)2)2⁽³⁺⁾*3ClO₄^(1-) = [Cu₅((C₄H₂O(CHNCH₂)(CHNCH₂CH₂))2)2(C₄N₃H₆)2][ClO₄]3 [ No CAS ]

References: [1]Journal of the Chemical Society. Chemical communications,1985,p. 262 - 263.

14
[ 7343-34-2 ]
[ 865-38-3 ]
[ 89210-86-6 ]

References: [1]Inorganic Chemistry,1984,vol. 23,p. 1404 - 1408.

15
ammonium thiocyanate [ No CAS ]
[ 7343-34-2 ]
cobalt(II) nitrate [ No CAS ]
[ 89210-77-5 ]

References: [1]Inorganic Chemistry,1984,vol. 23,p. 1404 - 1408.

16
ammonium thiocyanate [ No CAS ]
[ 7343-34-2 ]
nickel(II) nitrate [ No CAS ]
[ 89210-78-6 ]

References: [1]Inorganic Chemistry,1984,vol. 23,p. 1404 - 1408.

17
ammonium thiocyanate [ No CAS ]
[ 7343-34-2 ]
manganese(II) nitrate [ No CAS ]
[ 89231-70-9 ]

References: [1]Inorganic Chemistry,1984,vol. 23,p. 1404 - 1408.

18
[ 7343-34-2 ]
potassium borohydride [ No CAS ]
potassium hydrotris(3,5-dimethyl-1,2,4-triazol-1-yl)borate [ No CAS ]

References: [1]Inorganic Chemistry,1995,vol. 34,p. 5950 - 5962.
Inorg. Chem.,.
[2]Journal of Organometallic Chemistry,1996,vol. 506,p. 301 - 306.

19
[ 7343-34-2 ]
[ 557-42-6 ]
[ 89210-83-3 ]

References: [1]Inorganic Chemistry,1984,vol. 23,p. 1404 - 1408.

20
[ 7343-34-2 ]
potassium borohydride [ No CAS ]
potassium bis[hydrotris[3,5-dimethyl(1,2,4-triazolyl)]borato] [ No CAS ]

References: [1]Inorganic Chemistry Communications,2003,vol. 6,p. 408 - 411.

21
[ 7343-34-2 ]
[ 64-18-6 ]
zinc(II) oxide [ No CAS ]
[ 1146622-14-1 ]