Cas 1276112-73-2,(S)-methyl 4-([2-(1-methoxy-3-methyl-1-oxobutan-2-ylcarbamoyl)hydrazono]methyl)benzoate

1276112-73-2

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Basic information

Product Name: (S)-methyl 4-([2-(1-methoxy-3-methyl-1-oxobutan-2-ylcarbamoyl)hydrazono]methyl)benzoate
Synonyms: (S)-methyl 4-([2-(1-methoxy-3-methyl-1-oxobutan-2-ylcarbamoyl)hydrazono]methyl)benzoate
CAS NO:1276112-73-2
Molecular Formula:
Molecular Weight: 335.36
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: (S)-methyl 4-([2-(1-methoxy-3-methyl-1-oxobutan-2-ylcarbamoyl)hydrazono]methyl)benzoate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-methyl 4-([2-(1-methoxy-3-methyl-1-oxobutan-2-ylcarbamoyl)hydrazono]methyl)benzoate(1276112-73-2)
EPA Substance Registry System: (S)-methyl 4-([2-(1-methoxy-3-methyl-1-oxobutan-2-ylcarbamoyl)hydrazono]methyl)benzoate(1276112-73-2)

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: 1276112-73-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1276112-73-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,6,1,1 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1276112-73:
(9*1)+(8*2)+(7*7)+(6*6)+(5*1)+(4*1)+(3*2)+(2*7)+(1*3)=142
142 % 10 = 2
So 1276112-73-2 is a valid CAS Registry Number.

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1276112-73-2Relevant academic research and scientific papers

Semicarbazones from N-hydroxyureas and amines: A novel entry in the reactivity of the acyl nitroso group

Paz, Jairo,Perez-Balado, Carlos,Iglesias, Beatriz,Munoz, Luis

supporting information; experimental part, p. 1800 - 1803 (2011/06/10)

The condensation of carbamoyl nitroso compounds, obtained by oxidation of N-hydroxyureas, with amines unexpectedly afforded semicarbazones (aka carbamoyl hydrazones). Although the substitution of the nitrosyl moiety might compete to afford the correspondi

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