Cas 195626-05-2,(E)-(2R,4R)-6-Benzenesulfonyl-2-tert-butoxycarbonylamino-4-methyl-hex-5-enoic acid methyl ester

195626-05-2

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Basic information

Product Name: (E)-(2R,4R)-6-Benzenesulfonyl-2-tert-butoxycarbonylamino-4-methyl-hex-5-enoic acid methyl ester
Synonyms: (E)-(2R,4R)-6-Benzenesulfonyl-2-tert-butoxycarbonylamino-4-methyl-hex-5-enoic acid methyl ester
CAS NO:195626-05-2
Molecular Formula:
Molecular Weight: 397.492
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)-(2R,4R)-6-Benzenesulfonyl-2-tert-butoxycarbonylamino-4-methyl-hex-5-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(2R,4R)-6-Benzenesulfonyl-2-tert-butoxycarbonylamino-4-methyl-hex-5-enoic acid methyl ester(195626-05-2)
EPA Substance Registry System: (E)-(2R,4R)-6-Benzenesulfonyl-2-tert-butoxycarbonylamino-4-methyl-hex-5-enoic acid methyl ester(195626-05-2)

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: 195626-05-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 195626-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,6,2 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 195626-05:
(8*1)+(7*9)+(6*5)+(5*6)+(4*2)+(3*6)+(2*0)+(1*5)=162
162 % 10 = 2
So 195626-05-2 is a valid CAS Registry Number.

195626-05-2Upstream product

195626-05-2Downstream Products

195626-05-2Relevant academic research and scientific papers

Stereospecific Allylation of a Serine-derived Zinc/Copper Reagent. Synthesis of Substituted Pipecolic Acid Derivatives

Jackson, Richard F.W.,Turner, Debra,Block, Michael H.

, p. 789 - 790 (1997)

Serine-derived zinc/copper reagents 1 and 2 add to enantiomerically pure (η3-allyl)iron tetracarbonyl salts in fair to good yield in a stereospecific fashion. The vinylsulfones 10-12 can be converted into 4-methylpipecolic acid derivatives 19-21 in a two-step process comprising epoxidation and Zn/TMSCl mediated cyclisation.

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