Cas 1092115-96-2,1-phenylcarbamoylmethyl-1H-[1,2,3]triazole-4-carboxylic acid (4-methoxy-benzyloxy)-amide

1092115-96-2

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Basic information

Product Name: 1-phenylcarbamoylmethyl-1H-[1,2,3]triazole-4-carboxylic acid (4-methoxy-benzyloxy)-amide
Synonyms: 1-phenylcarbamoylmethyl-1H-[1,2,3]triazole-4-carboxylic acid (4-methoxy-benzyloxy)-amide
CAS NO:1092115-96-2
Molecular Formula:
Molecular Weight: 381.391
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-phenylcarbamoylmethyl-1H-[1,2,3]triazole-4-carboxylic acid (4-methoxy-benzyloxy)-amide(CAS DataBase Reference)
NIST Chemistry Reference: 1-phenylcarbamoylmethyl-1H-[1,2,3]triazole-4-carboxylic acid (4-methoxy-benzyloxy)-amide(1092115-96-2)
EPA Substance Registry System: 1-phenylcarbamoylmethyl-1H-[1,2,3]triazole-4-carboxylic acid (4-methoxy-benzyloxy)-amide(1092115-96-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1092115-96-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1092115-96-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,1,1 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1092115-96:
(9*1)+(8*0)+(7*9)+(6*2)+(5*1)+(4*1)+(3*5)+(2*9)+(1*6)=132
132 % 10 = 2
So 1092115-96-2 is a valid CAS Registry Number.

1092115-96-2Upstream product

10258-71-6 α-azidoacetanilide

1092115-96-2Downstream Products

1092115-68-8 1-phenylcarbamoylmethyl-1H-[1,2,3]triazole-4-carboxylic acid hydroxyamide

1092115-96-2Relevant academic research and scientific papers

Histone deacetylase inhibitors through click chemistry

Shen, Jie,Woodward, Robert,Kedenburg, James Patrick,Liu, Xianwei,Chen, Min,Fang, Lanyan,Sun, Duxin,Wang, Peng George

experimental part, p. 7417 - 7427 (2009/12/26)

Histone deacetylase inhibitors (HDACi) are a relatively new class of chemotherapy agents. Herein, we report a click-chemistry based approach to the synthesis of HDACi. Fourteen agents were synthesized from the combination of two alkyne and seven azido pre

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