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3-Hydroxymethyl-4-oxa-1-azabicyclo[3.2.0]heptan-7-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66036-39-3

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66036-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66036-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,3 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66036-39:
(7*6)+(6*6)+(5*0)+(4*3)+(3*6)+(2*3)+(1*9)=123
123 % 10 = 3
So 66036-39-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO3/c8-3-4-2-7-5(9)1-6(7)10-4/h4,6,8H,1-3H2/t4-,6+/m1/s1

66036-39-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R,5S)-3-(hydroxymethyl)-4-oxa-1-azabicyclo[3.2.0]heptan-7-one

1.2 Other means of identification

Product number -
Other names 2-Hydroxymethylclavam

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

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

More Details:66036-39-3 SDS

66036-39-3Relevant academic research and scientific papers

3-SUBSTITUTED-4-OXA-1-AZABICYCLO[3,2,0]HEPTAN-7-ONE AS CYSTEINE PROTEASE INHIBITORS

-

, (2008/06/13)

The use of certain 3-substituted-4-oxa-1-azabicyclo[3,2,0] heptan-7-one derivatives of general formula I, STR1 or physiologically acceptable salts thereof or isomers thereof, as active ingredients for the preparation of pharmaceutical composition and trea

Enantiocontrolled synthesis of the antifungal β-lactam (2R,5S)-2-(hydroxymethyl)clavam

Konosu,Oida

, p. 2212 - 2215 (2007/10/02)

The antifungal β-lactam (2R,5S)-2-(hydroxymethyl)clavam was synthesized in a convergent and stereocontrolled manner from methyl 6-phthalimidopenicillanate and 2,3-O-isopropylidene-(R)-glyceraldehyde. Convenient methods of acetonide cleavage and phthalimide deblocking are also described.

Total Synthesis of &β-Lactamase Inhibitors based on the 4-Oxa-1-azabicycloheptan-7-one Ring System

Bentley, Peter H.,Hunt, Eric

, p. 2222 - 2227 (2007/10/02)

4-(2-Bromoethoxy)azetidin-2-one (4), 4-(1,3-dibromoisopropoxy)azetidin-2-one (5), 4-(1-benzyloxy-3-chloroisopropoxy)azetidin-2-one (6), 4-azetidin-2-one (7), and 4-azetidin-2-one (8) have been s

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