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221349-56-0

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  • (3S,4S)-3-[(1S)-1,2-dihydroxyethyl]-1-(4-fluorophenyl)-4-(4-phenylmethoxyphenyl)azetidin-2-one

    Cas No: 221349-56-0

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221349-56-0 Usage

Uses

(3S,4S)-4-(4-(Benzyloxy)phenyl)-3-((S)-1,2-dihydroxyethyl)-1-(4-fluorophenyl)azetidin-2-one is a reactant in the synthesis of Sch 57939, a β-lactam-based cholesterol absorption inhibitor.

Check Digit Verification of cas no

The CAS Registry Mumber 221349-56-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,3,4 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 221349-56:
(8*2)+(7*2)+(6*1)+(5*3)+(4*4)+(3*9)+(2*5)+(1*6)=110
110 % 10 = 0
So 221349-56-0 is a valid CAS Registry Number.

221349-56-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4S)-3-[(1S)-1,2-dihydroxyethyl]-1-(4-fluorophenyl)-4-(4-phenylmethoxyphenyl)azetidin-2-one

1.2 Other means of identification

Product number -
Other names 2-AZETIDINONE,3-[(1S)-1,2-DIHYDROXYETHYL]-1-(4-FLUOROPHENYL)-4-[4-(PHENYLMETHOXY)PHENYL]-,(3S,4S)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:221349-56-0 SDS

221349-56-0Relevant articles and documents

A concise asymmetric synthesis of A β-lactam-based cholesterol absorption inhibitor

Wu, George Guangzhong

, p. 298 - 300 (2000)

A concise, four-step, asymmetric synthesis of β-lactam-based cholesterol absorption inhibitor, Sch 57939, was developed. The discovery of a one-step enantio- and diastereoselective synthesis of a trans-β-lactam provided easy access to the desired three chiral centers. A novel zinc phenoxide-promoted ether synthesis was reported for the completion of the side chain.

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