Cas 141320-40-3,(S)-2-Bromo-2-((S)-methoxy-phenyl-methyl)-3,3-dimethyl-butyric acid methyl ester

141320-40-3

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Basic information

Product Name: (S)-2-Bromo-2-((S)-methoxy-phenyl-methyl)-3,3-dimethyl-butyric acid methyl ester
Synonyms: (S)-2-Bromo-2-((S)-methoxy-phenyl-methyl)-3,3-dimethyl-butyric acid methyl ester
CAS NO:141320-40-3
Molecular Formula:
Molecular Weight: 329.234
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)-2-Bromo-2-((S)-methoxy-phenyl-methyl)-3,3-dimethyl-butyric acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-Bromo-2-((S)-methoxy-phenyl-methyl)-3,3-dimethyl-butyric acid methyl ester(141320-40-3)
EPA Substance Registry System: (S)-2-Bromo-2-((S)-methoxy-phenyl-methyl)-3,3-dimethyl-butyric acid methyl ester(141320-40-3)

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: 141320-40-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141320-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,2 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141320-40:
(8*1)+(7*4)+(6*1)+(5*3)+(4*2)+(3*0)+(2*4)+(1*0)=73
73 % 10 = 3
So 141320-40-3 is a valid CAS Registry Number.

141320-40-3Upstream product

67-56-1 methanol

141320-40-3Downstream Products

141320-47-0 2-(Methoxy-phenyl-methyl)-3,3-dimethyl-butyric acid methyl ester

141320-40-3Relevant academic research and scientific papers

The Use of Lewis Acids in Radical Chemistry. Chelation-Controlled Radical Reductions of Substituted α-Bromo-β-alkoxy Esters and Chelation-Controlled Radical Addition Reactions

Guindon, Yvan,Rancourt

, p. 6554 - 6565 (2007/10/03)

The radical reduction of a series of α-bromo-β-alkoxy esters under chelation-controlled conditions is reported. Proceeding with high stereoselectivity in the presence of MgBr2middot;OEt2, reductions give access to syn products. Syste

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