Biochemical Engineering

26198-19-6

  • Product Name:6-Chloro-1-hydroxibenzotriazol
  • Molecular Formula:C6H4 Cl N3 O
  • Specifications:99%
  • Molecular Weight:169.57
Inquiry

Product Details;

CasNo: 26198-19-6

Molecular Formula: C6H4 Cl N3 O

High Grade 99% Purity 6-Chloro-1-hydroxibenzotriazol 26198-19-6 Powder

  • Molecular Formula:C6H4 Cl N3 O
  • Molecular Weight:169.57
  • Vapor Pressure:2.66E-06mmHg at 25°C 
  • Melting Point:197 °C 
  • Refractive Index:1.758 
  • Boiling Point:379.5 °C at 760 mmHg 
  • PKA:6.69±0.58(Predicted) 
  • Flash Point:183.3 °C 
  • PSA:50.94000 
  • Density:1.71 g/cm3 
  • LogP:1.32200 

6-Chloro-1-hydroxibenzotriazol(Cas 26198-19-6) Usage

Chemical Properties

White powder

InChI:InChI=1/C6H4ClN3O/c7-4-1-2-5-6(3-4)10(11)9-8-5/h1-3,11H

26198-19-6 Relevant articles

Molybdenum-Catalyzed Deoxygenation of Heteroaromatic N-Oxides and Hydroxides using Pinacol as Reducing Agent

Rubio-Presa, Rubén,Fernández-Rodríguez, Manuel A.,Pedrosa, María R.,Arnáiz, Francisco J.,Sanz, Roberto

supporting information, p. 1752 - 1757 (2017/05/22)

A molybdenum-catalyzed deoxygenation of ...

Concerted amidation of activated esters: Reaction path and origins of selectivity in the kinetic resolution of cyclic amines via N-heterocyclic carbenes and hydroxamic acid cocatalyzed acyl transfer

Allen, Scott E.,Hsieh, Sheng-Ying,Gutierrez, Osvaldo,Bode, Jeffrey W.,Kozlowski, Marisa C.

supporting information, p. 11783 - 11791 (2014/11/08)

The N-heterocyclic carbene and hydroxami...

Spectrophotometric determination of pKa's of 1-Hydroxybenzotriazole and oxime derivatives in 95% acetonitrile-water

Fathalla, Magda Fouad,Khattab, Sherine Nabil

experimental part, p. 324 - 332 (2012/05/04)

1-hydroxybenzotriazole derivatives are u...

Synthesis and aminolysis of N,N-diethyl carbamic ester of HOBt derivatives

Khattab, Sherine Nabil,Hassan, Seham Yassin,Hamed, Ezzat Awad,Albericio, Fernando,Ayman, El-Faham

experimental part, p. 75 - 81 (2010/07/15)

The reaction of N,N-diethyl carbamates o...

26198-19-6 Process route

2,5-dichloronitrobenzene
89-61-2

2,5-dichloronitrobenzene

6-chloro-1-hydroxybenzotriazole
26198-19-6

6-chloro-1-hydroxybenzotriazole

Conditions
Conditions Yield
With hydrazine hydrate; In ethanol; for 36h; Reflux;
79%
With hydrazine hydrate; In ethanol; for 24h; Reflux;
piperidine
110-89-4

piperidine

6-chloro-1H-benzo[d][1,2,3]triazol-1-yl diethylcarbamate
1250853-37-2

6-chloro-1H-benzo[d][1,2,3]triazol-1-yl diethylcarbamate

N,N-diethylpiperidine-4-carboxamide
59486-99-6

N,N-diethylpiperidine-4-carboxamide

6-chloro-1-hydroxybenzotriazole
26198-19-6

6-chloro-1-hydroxybenzotriazole

Conditions
Conditions Yield
In acetonitrile; at 30 ℃; Temperature; Kinetics;

26198-19-6 Upstream products

  • 110-89-4
    110-89-4

    piperidine

  • 1250853-37-2
    1250853-37-2

    6-chloro-1H-benzo[d][1,2,3]triazol-1-yl diethylcarbamate

  • 110-91-8
    110-91-8

    morpholine

  • 89-61-2
    89-61-2

    2,5-dichloronitrobenzene

26198-19-6 Downstream products

  • 89028-38-6
    89028-38-6

    1,1'-di(6-chlorobenzotriazolo) oxallate(Cl-DBTO)

  • 70082-89-2
    70082-89-2

    (S)-2-Benzyloxycarbonylamino-3-methyl-butyric acid 6-chloro-benzotriazol-1-yl ester

  • 59577-40-1
    59577-40-1

    6-chloro-1H-benzo[d][1,2,3]triazol-1-yl ethyl carbonate

  • 59577-30-9
    59577-30-9

    1-tert-butoxycarbonyloxy-6-chloro-1H-benzotriazole

Relevant Products