Cas 127392-90-9,[(S)-3-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ<sup>6</sup>-thia-4-aza-tricyclo[5.2.1.0<sup>1,5</sup>]dec-4-yl)-2-methyl-3-oxo-propyl]-methyl-carbamic acid benzyl ester

127392-90-9

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Basic information

Product Name: [(S)-3-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-2-methyl-3-oxo-propyl]-methyl-carbamic acid benzyl ester
Synonyms:
CAS NO:127392-90-9
Molecular Formula:
Molecular Weight: 448.583
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)-3-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-2-methyl-3-oxo-propyl]-methyl-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-3-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-2-methyl-3-oxo-propyl]-methyl-carbamic acid benzyl ester(127392-90-9)
EPA Substance Registry System: [(S)-3-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-2-methyl-3-oxo-propyl]-methyl-carbamic acid benzyl ester(127392-90-9)

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: 127392-90-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127392-90-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,3,9 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 127392-90:
(8*1)+(7*2)+(6*7)+(5*3)+(4*9)+(3*2)+(2*9)+(1*0)=139
139 % 10 = 9
So 127392-90-9 is a valid CAS Registry Number.

127392-90-9Upstream product

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127392-90-9Relevant academic research and scientific papers

ASYMMETRIC ALKYLATION OF N-ACYLSULTAMS: A GENERAL ROUTE TO ENANTIOMERICALLY PURE, CRYSTALLINE C(α,α)-DISUBSTITUTED CARBOXYLIC ACID DERIVATIVES.

Oppolzer, Wolfgang,Moretti, Robert,Thomi, Silvia

, p. 5603 - 5606 (2007/10/02)

Successive treatment of acylsultams 2 with nBuLi or NHMDS and primary alkyl halides, followed by crystallization, gave pure C(α)-alkylation products 4 and, via their non-destructive cleavage, enantiomerically pure alcohols 5 or carboxylic acids 6.

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