Cas 1192297-95-2,4-((2-(4-(4-boroxophenyl)-1H-1,2,3-triazol-1-yl)acetamido)methyl)phenylboronic acid

1192297-95-2

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Basic information

Product Name: 4-((2-(4-(4-boroxophenyl)-1H-1,2,3-triazol-1-yl)acetamido)methyl)phenylboronic acid
Synonyms: 4-((2-(4-(4-boroxophenyl)-1H-1,2,3-triazol-1-yl)acetamido)methyl)phenylboronic acid
CAS NO:1192297-95-2
Molecular Formula:
Molecular Weight: 379.976
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: 4-((2-(4-(4-boroxophenyl)-1H-1,2,3-triazol-1-yl)acetamido)methyl)phenylboronic acid(CAS DataBase Reference)
NIST Chemistry Reference: 4-((2-(4-(4-boroxophenyl)-1H-1,2,3-triazol-1-yl)acetamido)methyl)phenylboronic acid(1192297-95-2)
EPA Substance Registry System: 4-((2-(4-(4-boroxophenyl)-1H-1,2,3-triazol-1-yl)acetamido)methyl)phenylboronic acid(1192297-95-2)

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: 1192297-95-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1192297-95-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,2,9 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1192297-95:
(9*1)+(8*1)+(7*9)+(6*2)+(5*2)+(4*9)+(3*7)+(2*9)+(1*5)=182
182 % 10 = 2
So 1192297-95-2 is a valid CAS Registry Number.

1192297-95-2Upstream product

1192297-87-2 C₉H₁₁BN₄O₃

1192297-95-2Downstream Products

1192297-95-2Relevant academic research and scientific papers

Fluoride protects boronic acids in the copper(i)-mediated click reaction

Jin, Shan,Choudhary, Gaurav,Cheng, Yunfeng,Dai, Chaofeng,Li, Minyong,Wang, Binghe

supporting information; experimental part, p. 5251 - 5253 (2010/01/31)

Fluoride has been found to protect boronic acids from copper(i)-mediated decomposition; such findings should be very useful for the preparation of boronic acid-based carbohydrate sensors and boronic acid conjugates using the copper(i)-mediated click react

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