Cas 127392-96-5,(S)-2-Benzyloxy-1-((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)-3-phenyl-propan-1-one

127392-96-5

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Basic information

Product Name: (S)-2-Benzyloxy-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-phenyl-propan-1-one
Synonyms:
CAS NO:127392-96-5
Molecular Formula:
Molecular Weight: 453.602
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-Benzyloxy-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-phenyl-propan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-Benzyloxy-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-phenyl-propan-1-one(127392-96-5)
EPA Substance Registry System: (S)-2-Benzyloxy-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-phenyl-propan-1-one(127392-96-5)

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: 127392-96-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127392-96-5 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 127392-96:
(8*1)+(7*2)+(6*7)+(5*3)+(4*9)+(3*2)+(2*9)+(1*6)=145
145 % 10 = 5
So 127392-96-5 is a valid CAS Registry Number.

127392-96-5Upstream product

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127392-96-5Relevant 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 (1989)

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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