Cas 953053-77-5,(E)-4-[[2-(Benzyloxyimino-methyl)-phenyl]-(toluene-4-sulfonyl)-amino]-but-2-enoic acid ethyl ester

953053-77-5

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Basic information

Product Name: (E)-4-[[2-(Benzyloxyimino-methyl)-phenyl]-(toluene-4-sulfonyl)-amino]-but-2-enoic acid ethyl ester
Synonyms: (E)-4-[[2-(Benzyloxyimino-methyl)-phenyl]-(toluene-4-sulfonyl)-amino]-but-2-enoic acid ethyl ester
CAS NO:953053-77-5
Molecular Formula:
Molecular Weight: 492.596
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: (E)-4-[[2-(Benzyloxyimino-methyl)-phenyl]-(toluene-4-sulfonyl)-amino]-but-2-enoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-4-[[2-(Benzyloxyimino-methyl)-phenyl]-(toluene-4-sulfonyl)-amino]-but-2-enoic acid ethyl ester(953053-77-5)
EPA Substance Registry System: (E)-4-[[2-(Benzyloxyimino-methyl)-phenyl]-(toluene-4-sulfonyl)-amino]-but-2-enoic acid ethyl ester(953053-77-5)

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: 953053-77-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 953053-77-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,3,0,5 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 953053-77:
(8*9)+(7*5)+(6*3)+(5*0)+(4*5)+(3*3)+(2*7)+(1*7)=175
175 % 10 = 5
So 953053-77-5 is a valid CAS Registry Number.

953053-77-5Upstream product

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953053-77-5Relevant academic research and scientific papers

A formal synthesis of martinelline via a combination of two types of radical reactions

Takeda, Yoshifumi,Nakabayashi, Toshiki,Shirai, Atsushi,Fukumoto, Daisuke,Kiguchi, Toshiko,Naito, Takeaki

, p. 3481 - 3484 (2004)

A formal synthesis of martinelline has been accomplished via two types of radical reactions as the key steps. These are the radical addition-cyclization- elimination of an oxime ether carrying an unsaturated ester and a C-C bond formation through a radica

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