Cas 215796-35-3,2-[3-(2-Bromo-benzyl)-pent-4-ynyl]-malonic acid dimethyl ester

215796-35-3

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Basic information

Product Name: 2-[3-(2-Bromo-benzyl)-pent-4-ynyl]-malonic acid dimethyl ester
Synonyms: 2-[3-(2-Bromo-benzyl)-pent-4-ynyl]-malonic acid dimethyl ester
CAS NO:215796-35-3
Molecular Formula:
Molecular Weight: 367.239
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: 2-[3-(2-Bromo-benzyl)-pent-4-ynyl]-malonic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[3-(2-Bromo-benzyl)-pent-4-ynyl]-malonic acid dimethyl ester(215796-35-3)
EPA Substance Registry System: 2-[3-(2-Bromo-benzyl)-pent-4-ynyl]-malonic acid dimethyl ester(215796-35-3)

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: 215796-35-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 215796-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,7,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 215796-35:
(8*2)+(7*1)+(6*5)+(5*7)+(4*9)+(3*6)+(2*3)+(1*5)=153
153 % 10 = 3
So 215796-35-3 is a valid CAS Registry Number.

215796-35-3Upstream product

108-59-8 malonic acid dimethyl ester

215796-35-3Downstream Products

215796-36-4 2-[3-(2-Bromo-benzyl)-pent-4-enyl]-malonic acid dimethyl ester

215796-35-3Relevant academic research and scientific papers

Directed palladium-catalyzed cascade cyclization as an approach to trans- and cis-hexahydro-1H-benz[f]indenes

Coudanne, Isabelle,Balme, Geneviève

, p. 998 - 1000 (1998)

The hydrogenation of the acetylenic substrate 6 followed by a palladium-catalyzed cascade bis-cyclization process led to a trans-hexahydro-1H-benz[f]indene. By changing the order of the two preceding steps, only the cis-hexahydro-1H-benz[f]indene structur

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