Cas 158835-81-5,2-diazo-N-<2-(3,4-dimethoxyphenyl)ethyl>-N-(5-methylhex-5-enoyl)malonamic acid ethyl ester

158835-81-5

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Basic information

Product Name: 2-diazo-N-<2-(3,4-dimethoxyphenyl)ethyl>-N-(5-methylhex-5-enoyl)malonamic acid ethyl ester
Synonyms: 2-diazo-N-<2-(3,4-dimethoxyphenyl)ethyl>-N-(5-methylhex-5-enoyl)malonamic acid ethyl ester
CAS NO:158835-81-5
Molecular Formula:
Molecular Weight: 431.489
EINECS: N/A
Product Categories: N/A
Mol File: 158835-81-5.mol
Article Data: 1

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: 2-diazo-N-<2-(3,4-dimethoxyphenyl)ethyl>-N-(5-methylhex-5-enoyl)malonamic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-diazo-N-<2-(3,4-dimethoxyphenyl)ethyl>-N-(5-methylhex-5-enoyl)malonamic acid ethyl ester(158835-81-5)
EPA Substance Registry System: 2-diazo-N-<2-(3,4-dimethoxyphenyl)ethyl>-N-(5-methylhex-5-enoyl)malonamic acid ethyl ester(158835-81-5)

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: 158835-81-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 158835-81-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,8,3 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 158835-81:
(8*1)+(7*5)+(6*8)+(5*8)+(4*3)+(3*5)+(2*8)+(1*1)=175
175 % 10 = 5
So 158835-81-5 is a valid CAS Registry Number.

158835-81-5Upstream product

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158835-81-5Relevant articles and documents

Tandem dipolar cycloaddition - Mannich cyclization as an approach to tricyclic nitrogen heterocycles

Padwa,Brodney,Marino J.P.,Osterhout,Price

, p. 67 - 77 (2007/10/03)

A series of 2-diazo-N-[2-(3,4-dimethoxyphenyl)ethyl]-N-hept-6-enoylmalonamides were prepared and treated with a catalytic amount of rhodium(II) perfluorobutyrate. The resultant carbenoids undergo facile cyclization onto the neighboring amide carbonyl oxyg

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