Cas 119105-92-9,N'-(2-Hydroxy-2-p-tolyl-acetyl)-hydrazinecarboxylic acid methyl ester

119105-92-9

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Basic information

Product Name: N'-(2-Hydroxy-2-p-tolyl-acetyl)-hydrazinecarboxylic acid methyl ester
Synonyms: N'-(2-Hydroxy-2-p-tolyl-acetyl)-hydrazinecarboxylic acid methyl ester
CAS NO:119105-92-9
Molecular Formula:
Molecular Weight: 238.243
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: N'-(2-Hydroxy-2-p-tolyl-acetyl)-hydrazinecarboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N'-(2-Hydroxy-2-p-tolyl-acetyl)-hydrazinecarboxylic acid methyl ester(119105-92-9)
EPA Substance Registry System: N'-(2-Hydroxy-2-p-tolyl-acetyl)-hydrazinecarboxylic acid methyl ester(119105-92-9)

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: 119105-92-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 119105-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,1,0 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 119105-92:
(8*1)+(7*1)+(6*9)+(5*1)+(4*0)+(3*5)+(2*9)+(1*2)=109
109 % 10 = 9
So 119105-92-9 is a valid CAS Registry Number.

119105-92-9Upstream product

119105-92-9Downstream Products

18584-20-8 4-methylmandelic acid

119105-92-9Relevant academic research and scientific papers

SYNTHESE EN UNE ETAPE D'α-ALCOXYHYDRAZIDES, DE DERIVES D'α-AMINOACIDES ET D'α-HYDROXYACIDES A PARTIR DES α-HALOGENOHYDRAZIDES. ETUDE DU MECANISME DE LA REACTION.

Legrel, P.,Baudy-Floc'h, M.,Robert, A.

, p. 4805 - 4814 (2007/10/02)

α-Halohydrazides react with nucleophiles under basic conditions to give α-functionalized hydrazides.We have shown that this reaction is not a direct nucleophilic substitution of the halogen but more likely proceeds through the formation of an aziridinone

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