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107833-73-8

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107833-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107833-73-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,3 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107833-73:
(8*1)+(7*0)+(6*7)+(5*8)+(4*3)+(3*3)+(2*7)+(1*3)=128
128 % 10 = 8
So 107833-73-8 is a valid CAS Registry Number.

107833-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitropropanal diethyl acetal

1.2 Other means of identification

Product number -
Other names 1,1-Diethoxy-3-nitropropane

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:107833-73-8 SDS

107833-73-8Downstream Products

107833-73-8Relevant articles and documents

Synthetic studies on statins. Part 1: A short and cyanide-free synthesis of atorvastatin calcium via an enantioselective aldol strategy

Hu, Lemeng,Xiong, Fangjun,Chen, Xiaofei,Chen, Wenxue,He, Qiuqin,Chen, Fener

, p. 207 - 211 (2013/04/10)

A short and cyanide-free enantioselective synthesis of atorvastatin calcium has been achieved starting from a commercially available highly substituted 1,4-diketone in an overall yield of 40%. The key step in this approach is the asymmetric aldol reaction of an aldehyde with diketene in the presence of Ti(O-i-Pr)4-Schiff base complex to create the (5R)-stereochemistry of atorvastatin calcium.

3-Nitropropanal and 3-Nitropropanol: Preparation of the Parent Compounds and Derivatives

Oehrlein, Reinhold,Schwab, Wilfried,Ehrler, Rudolf,Jaeger, Volker

, p. 535 - 538 (2007/10/02)

3-Nitropropanal has been prepared for the first time by 1,4-nitrite addition to acrolein.Several acetals of 3-nitropropanal are described, as well as 3-nitropropanol and some of its ethers. 3-Nitropropanol has been obtained by borane-dimethyl sulfide reduction of both 3-nitropropanal and 3-nitropropanoic acid.These reactions make available a variety of nitro compounds known as, or expected to become, highly useful and versatile building blocks for organic syntheses.

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