Cas 1359827-72-7,(2R,3S)-diethyl 3-(3-bromophenyl)-2-formyl-cyclopropane-1,1-dicarboxylate

1359827-72-7

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Basic information

Product Name: (2R,3S)-diethyl 3-(3-bromophenyl)-2-formyl-cyclopropane-1,1-dicarboxylate
Synonyms: (2R,3S)-diethyl 3-(3-bromophenyl)-2-formyl-cyclopropane-1,1-dicarboxylate
CAS NO:1359827-72-7
Molecular Formula:
Molecular Weight: 369.212
EINECS: N/A
Product Categories: N/A
Mol File: 1359827-72-7.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: (2R,3S)-diethyl 3-(3-bromophenyl)-2-formyl-cyclopropane-1,1-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S)-diethyl 3-(3-bromophenyl)-2-formyl-cyclopropane-1,1-dicarboxylate(1359827-72-7)
EPA Substance Registry System: (2R,3S)-diethyl 3-(3-bromophenyl)-2-formyl-cyclopropane-1,1-dicarboxylate(1359827-72-7)

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: 1359827-72-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1359827-72-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,9,8,2 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1359827-72:
(9*1)+(8*3)+(7*5)+(6*9)+(5*8)+(4*2)+(3*7)+(2*7)+(1*2)=207
207 % 10 = 7
So 1359827-72-7 is a valid CAS Registry Number.

1359827-72-7Upstream product

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1359827-72-7Relevant articles and documents

Asymmetric oxidative Lewis base catalysis - Unifying iminium and enamine organocatalysis with oxidations

Rueping, Magnus,Sunden, Henrik,Hubener, Lukas,Sugiono, Erli

supporting information; experimental part, p. 2201 - 2203 (2012/03/09)

Enantioselective oxidative domino reactions of allylic alcohols to functionalized aldehydes have been developed. The one pot domino oxidation-iminium activation represents a convenient strategy for the enantioselective addition of malonates to allylic alc

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