Cas 183074-45-5,Acetic acid (3R,4S)-1-((1S,4R)-7,7-dimethyl-2-oxo-bicyclo[2.2.1]hept-1-ylmethanesulfonyl)-2-oxo-4-phenyl-azetidin-3-yl ester

183074-45-5

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Basic information

Product Name: Acetic acid (3R,4S)-1-((1S,4R)-7,7-dimethyl-2-oxo-bicyclo[2.2.1]hept-1-ylmethanesulfonyl)-2-oxo-4-phenyl-azetidin-3-yl ester
Synonyms:
CAS NO:183074-45-5
Molecular Formula:
Molecular Weight: 419.499
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: Acetic acid (3R,4S)-1-((1S,4R)-7,7-dimethyl-2-oxo-bicyclo[2.2.1]hept-1-ylmethanesulfonyl)-2-oxo-4-phenyl-azetidin-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (3R,4S)-1-((1S,4R)-7,7-dimethyl-2-oxo-bicyclo[2.2.1]hept-1-ylmethanesulfonyl)-2-oxo-4-phenyl-azetidin-3-yl ester(183074-45-5)
EPA Substance Registry System: Acetic acid (3R,4S)-1-((1S,4R)-7,7-dimethyl-2-oxo-bicyclo[2.2.1]hept-1-ylmethanesulfonyl)-2-oxo-4-phenyl-azetidin-3-yl ester(183074-45-5)

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: 183074-45-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 183074-45-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,0,7 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 183074-45:
(8*1)+(7*8)+(6*3)+(5*0)+(4*7)+(3*4)+(2*4)+(1*5)=135
135 % 10 = 5
So 183074-45-5 is a valid CAS Registry Number.

183074-45-5Upstream product

183074-45-5Downstream Products

15399-05-0 ethyl (R)-2-hydroxy-3-phenylpropanoate

183074-45-5Relevant academic research and scientific papers

Asymmetric synthesis of α-hydroxy acids via β-lactams

Srirajan,Deshmukh,Puranik,Bhawal

, p. 2733 - 2738 (1996)

A diastereoselective synthesis of β-lactams 5a-e and 6a-e has been achieved, via a Staudinger reaction using imines derived from (1S)-(+)-camphor-10-sulfonamide, in good yields. The major diastereomers 6a-e were isolated in pure form by crystallization. T

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