Cas 195380-84-8,[(S)-1-((R)-1,2-Dihydroxy-ethyl)-butyl]-carbamic acid tert-butyl ester

195380-84-8

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Basic information

Product Name: [(S)-1-((R)-1,2-Dihydroxy-ethyl)-butyl]-carbamic acid tert-butyl ester
Synonyms: [(S)-1-((R)-1,2-Dihydroxy-ethyl)-butyl]-carbamic acid tert-butyl ester
CAS NO:195380-84-8
Molecular Formula:
Molecular Weight: 233.308
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)-1-((R)-1,2-Dihydroxy-ethyl)-butyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-1-((R)-1,2-Dihydroxy-ethyl)-butyl]-carbamic acid tert-butyl ester(195380-84-8)
EPA Substance Registry System: [(S)-1-((R)-1,2-Dihydroxy-ethyl)-butyl]-carbamic acid tert-butyl ester(195380-84-8)

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: 195380-84-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 195380-84-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,3,8 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 195380-84:
(8*1)+(7*9)+(6*5)+(5*3)+(4*8)+(3*0)+(2*8)+(1*4)=168
168 % 10 = 8
So 195380-84-8 is a valid CAS Registry Number.

195380-84-8Upstream product

92418-71-8 (2R,3R)-2,3-epoxy-1-hexanol

195380-84-8Downstream Products

195380-84-8Relevant academic research and scientific papers

Design and synthesis of new secretory phospholipase A2 inhibitor of a phospholipid analog

Iwama, Seiji,Segawa, Masaki,Fujii, Shinobu,Ikeda, Kiyoshi,Katsumura, Shigeo

, p. 3495 - 3498 (1998)

All stereoisomers of N-acyl-4,5-disubstituted oxazolidinone phospholipid analogs were synthesized by regio and stereoselective epoxide ring opening accompanied by introduction of an amino group. The (4R,5S)-derivative showed stronger inhibitory activity toward type II phospholipase A2 than the 4- substituted oxazolidinone phospholipid analog previously reported.

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