Cas 134051-01-7,1H-1,2,3-Triazole-4-carboxylicacid,1-(phenylamino)-(9CI)

134051-01-7

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Basic information

Product Name: 1H-1,2,3-Triazole-4-carboxylicacid,1-(phenylamino)-(9CI)
Synonyms: 1H-1,2,3-Triazole-4-carboxylicacid,1-(phenylamino)-(9CI)
CAS NO:134051-01-7
Molecular Formula: C₉H₈N₄O₂
Molecular Weight: 204.18542
EINECS: N/A
Product Categories: AMINOACID
Mol File: 134051-01-7.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 446.1±37.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.45±0.1 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 3.56±0.50(Predicted)
CAS DataBase Reference: 1H-1,2,3-Triazole-4-carboxylicacid,1-(phenylamino)-(9CI)(CAS DataBase Reference)
NIST Chemistry Reference: 1H-1,2,3-Triazole-4-carboxylicacid,1-(phenylamino)-(9CI)(134051-01-7)
EPA Substance Registry System: 1H-1,2,3-Triazole-4-carboxylicacid,1-(phenylamino)-(9CI)(134051-01-7)

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: 134051-01-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134051-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,0,5 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 134051-01:
(8*1)+(7*3)+(6*4)+(5*0)+(4*5)+(3*1)+(2*0)+(1*1)=77
77 % 10 = 7
So 134051-01-7 is a valid CAS Registry Number.

134051-01-7Upstream product

134050-91-2 5-Chloro-1,2,3-thiadiazole-4-carbaldehyde N-phenylhydrazone

134051-01-7Downstream Products

134051-03-9 1-Phenylamino-1H-[1,2,3]triazole-4-carboxylic acid methyl ester

134051-01-7Relevant academic research and scientific papers

Ring Transformations of 5-Chloro-1,2,3-thiadiazole-4-carbaldehyde with Amines, Hydrazines and Hydroxylamine

L'abbe, Gerrit,Vanderstede, Els,Dehaen, Wim,Delbeke, Pieter,Toppet, Suzanne

, p. 607 - 610 (2007/10/02)

5-Chloro-1,2,3-thiadiazole-4-carbaldehyde, prepared in four steps from 1,3-dichloroacetone, reacts with alkyl- and aryl-amines in alcohol solution to give 1,2,3-triazole-4-thiocarboxamides 9a-f.Similarly, hydrazine and N-aminomorpholine furnish the 1,2,3-

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