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3-(Chloromethyl)-1-methyl-1H-1,2,4-triazole hydrochloride

Detailed Information

  • Product Name:3-(Chloromethyl)-1-methyl-1H-1,2,4-triazole hydrochloride
  • CasNo.:135206-76-7
  • MF:C4H6ClN3
  • MW:168.026

pd_nature

  • Purity:99%
  • pd_boiling:
  • Packing:
  • Throughput:

Product Details;

CasNo： 135206-76-7

MF： C4H6ClN3

Cosmetics Grade 3-(Chloromethyl)-1-methyl-1H-1,2,4-triazole hydrochloride 135206-76-7 For Sale with Good Price

  • Molecular Formula:C4H6ClN3*ClH
  • Molecular Weight:168.026
  • Vapor Pressure:0.0164mmHg at 25°C 
  • Refractive Index:1.595 
  • Boiling Point:255.3 °C at 760 mmHg 
  • Flash Point:108.2 °C 
  • PSA：30.71000 
  • Density:1.36 g/cm3 
  • LogP:0.55390 

3-CHLOROMETHYL-1-METHYL-1H-[1,2,4]TRIAZOLE(Cas 135206-76-7) Usage

InChI:InChI=1/C4H6ClN3/c1-8-3-6-4(2-5)7-8/h3H,2H2,1H3

135206-76-7 Relevant articles

DIACYLGLYCEROL ACYLTRANSFERASE 2 INHIBITORS

-

Page/Page column 110; 111, (2013/10/22)

Derivatives of purine, 3H-imidazo[4,5-b]...

Pyrazolo-triazine derivatives as ligands for GABA receptors

-

, (2008/06/13)

Compounds according to Formula (I): or a...

Optically active antifungal azoles. III. Synthesis and antifungal activity of sulfide and sulfonamide derivatives of (2R,3R)-2-(2,4-difluorophenyl)-3- mercapto-1-(1H-1,2,4-triazol-1-yl)-2-butanol

Tasaka,Teranishi,Matsushita,Tamura,Hayashi,Okonogi,Itoh

, p. 85 - 94 (2007/10/02)

In an effort to find potent antifungal a...

Heteroaryliumthio substituted carbapenem derivatives: Synthesis and in vitro activity of 1β-methyl-2-(dihydropyrrolotriazoliumthio)carbapenems

Wildonger,Ratcliffe

, p. 1866 - 1882 (2007/10/02)

The syntheses of five thiols, including ...

135206-76-7 Process route

1-methyl-1H-[1,2,4]-(triazol-5-yl)methanol
91616-36-3

1-methyl-1H-[1,2,4]-(triazol-5-yl)methanol

3-chloromethyl-2-methyl-2H-[1,2,4]triazole hydrochloride
135206-76-7

3-chloromethyl-2-methyl-2H-[1,2,4]triazole hydrochloride

Conditions
Conditions Yield
With thionyl chloride; for 0.333333h; Yield given; Heating;
In thionyl chloride;
With thionyl chloride; In dichloromethane;
With thionyl chloride; at 0 - 80 ℃;
(1-methyl-1H-[1,2,4]-triazol-3-yl)methanol
135242-93-2

(1-methyl-1H-[1,2,4]-triazol-3-yl)methanol

3-chloromethyl-1-methyl-1H-[1,2,4]triazole hydrochloride
135206-76-7

3-chloromethyl-1-methyl-1H-[1,2,4]triazole hydrochloride

Conditions
Conditions Yield
With thionyl chloride; for 0.666667h; Heating;
90%

135206-76-7 Upstream products

  • 135242-93-2
    135242-93-2

    (1-methyl-1H-[1,2,4]-triazol-3-yl)methanol

  • 91616-36-3
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    1-methyl-1H-[1,2,4]-(triazol-5-yl)methanol

135206-76-7 Downstream products

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    5-Hydroxymethyl-3-(1-methyl-1H-[1,2,4]triazol-3-ylmethoxy)-4-phenylpyrazole

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    3-tert-butyl-7-(5-methylisoxazol-3-yl)-2-(1-methyl-1H-1,2,4-triazol-5-ylmethoxy)pyrazolo[1,5-d][1,2,4]triazine

  • 265642-78-2
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    3-bromo-7-(2-fluorophenyl)-2-(2-methyl-2H-[1,2,4]triazol-3-ylmethoxy)pyrazolo[1,5-d][1,2,4]triazine

  • 327985-57-9
    327985-57-9

    3,8-bis(2-fluorophenyl)-5-methyl-2-(2-methyl-2H-[1,2,4]triazol-3-ylmethoxy)imidazo[1,2-d][1,2,4]triazine

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