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3-Oxazolidinecarboxaldehyde,2,2-dimethyl-4-(1-methylethyl)-,(S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124716-44-5

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124716-44-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124716-44-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,7,1 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 124716-44:
(8*1)+(7*2)+(6*4)+(5*7)+(4*1)+(3*6)+(2*4)+(1*4)=115
115 % 10 = 5
So 124716-44-5 is a valid CAS Registry Number.

124716-44-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (5S)-N-formyl-2,2-dimethyl-5-isopropyl-1,3-oxazolidine

1.2 Other means of identification

Product number -
Other names (S)-4-Isopropyl-2,2-dimethyl-oxazolidine-3-carbaldehyde

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:124716-44-5 SDS

124716-44-5Relevant academic research and scientific papers

Synthesis of optically active β-lactams by the photolytic reaction of imines with optically active chromium carbene complexes

Hegedus,Imwinkelried,Alarid-Sargent,Dvorak,Satoh

, p. 1109 - 1117 (2007/10/02)

Optically active chromium carbene complexes utilizing (S)-valine- and (R)-phenylglycine-derived chiral auxillaries were synthesized and subjected to photolytic reaction with a number of imines. Optically active β-lactams were produced in good to excellent chemical yield and with high diastereoisomeric excess. Procedures for removal of the chiral auxillary to produce the optically active free amino β-lactams were developed.

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