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Butanoic acid, (3-bromo-4,5-dihydro-5-isoxazolyl)methyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140384-87-8

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140384-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140384-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,3,8 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 140384-87:
(8*1)+(7*4)+(6*0)+(5*3)+(4*8)+(3*4)+(2*8)+(1*7)=118
118 % 10 = 8
So 140384-87-8 is a valid CAS Registry Number.

140384-87-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Butyric acid (S)-3-bromo-4,5-dihydro-isoxazol-5-ylmethyl ester

1.2 Other means of identification

Product number -
Other names -

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:140384-87-8 SDS

140384-87-8Relevant academic research and scientific papers

Synthesis and pharmacological investigation of new chiral muscarinic antagonists

Carnielli,De Amici,De Micheli,Gianferrara,Maurich,Zacchigna,Grana,Boselli

, p. 21 - 27 (2007/10/02)

The two pairs of enantiomers of isoxazolidin-3-ones 3 and 4 were synthesized by means of Lipase PS-catalyzed hydrolyses of suitable racemic butyrates. The same butyrates were also employed as key intermediates in the preparation of racemic 3 and 4. The an

Nitrile Oxides in Medicinal Chemistry. 4. Chemoenzymatic Synthesis of Chiral Heterocyclic Derivatives

Amici, Marco De,Magri, Paolo,Micheli, Carlo De,Cateni, Francesca,Bovara, Roberto,et al.

, p. 2825 - 2829 (2007/10/02)

The two enantiomers of 3-bromo-5-(hydroxymethyl)-Δ2-isoxazoline (1) and 2-phenyl-5-(hydroxymethyl)-isoxazolidin-3-one (9) have been prepared in enantiomeric excess higher than 90percent by hydrolysis of the corresponding butyrates under the cat

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