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1070-13-9

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1070-13-9 Usage

General Description

2-PROPYLACROLEIN, also known as 2-propen-1-one, is a chemical compound with the molecular formula C6H10O. It is a colorless, flammable liquid with a pungent odor, and it is used in the production of polymers and coatings. 2-PROPYLACROLEIN is also used as a chemical intermediate in the manufacture of pharmaceuticals and other organic compounds. It is considered to be a hazardous substance and should be handled with caution due to its flammability and potential health risks. Additionally, it is not considered to be readily biodegradable and may persist in the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 1070-13-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1070-13:
(6*1)+(5*0)+(4*7)+(3*0)+(2*1)+(1*3)=39
39 % 10 = 9
So 1070-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O/c1-3-4-6(2)5-7/h5H,2-4H2,1H3

1070-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylidenepentanal

1.2 Other means of identification

Product number -
Other names 2-n-propylacrolein

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:1070-13-9 SDS

1070-13-9Related news

Mutagenicity of 2-methylacrolein, 2-ethylacrolein and 2-PROPYLACROLEIN (cas 1070-13-9) in Salmonella typhimurium TA 100. A comparative study07/25/2019

The C2-alkylated acrolein derivatives 2-methylacrolein, 2-ethylacrolein and 2-propylacrolein are mutagenic in Salmonella typhimurium TA100. They are direct mutagens, their mutagenic potency being inversely proportional to the size of the alkylating substituent in the C2 position. In the presence...detailed

1070-13-9Relevant articles and documents

Formal synthesis of brivaracetam: A key to construct the pyrrolidone scaffold using Pd-catalyzed oxidative cyclization and ring-closing metathesis reaction

Chavan, Subhash P.,Kawale, Sanket A.,Chavan, Prakash N.

, (2019)

A short and efficient synthetic approach for brivaracetam has been accomplished via two different routes which utilize Pd-catalyzed oxidative cyclization and ring-closing metathesis (RCM) as the key reaction. These two routes are novel, simple, scalable and rely on (E)-pent-2-en-1-ol and valeraldehyde as a commercially available starting material to yield brivaracetam with good overall yield.

Three Ways Aliphatic Aldehydes React with Nonstabilized Azomethine Ylides

Buev, Evgeny M.,Gorbunova, Evgeniya V.,Moshkin, Vladimir S.,Sosnovskikh, Vyacheslav Y.

, p. 343 - 348 (2020)

Aliphatic aldehydes readily react with nonstabilized azomethine ylides in one of the three ways to give oxazolidines, pyrrolidines, or Mannich bases, depending on the structure of the starting compound and the reaction conditions. The use of N -(methoxymethyl)- N -[(trimethylsilyl)methyl]benzylamine in DMF provided 5-alkyloxazolidines in 40-97percent yields. On the other hand, three-component reactions of aliphatic aldehydes bearing one α-hydrogen with N -methyl(benzyl)glycine and formaldehyde gives Mannich bases in yields of 47-98percent. A similar reaction of aldehydes bearing branched alkyl groups and two hydrogen atoms at the α-position proceeds as a domino process that gives 3-alkyl-3-formylpyrrolidines in yields of 34-93percent.

Substituted thiophene and benzoquinone and isoxazole compound and its preparation method and application

-

Paragraph 0176; 0177, (2017/07/23)

The invention relates to the technical field of medicine, and provides substituted tricyclo-quinone compounds and pharmaceutically acceptable salts thereof. The structural general formula of the substituted aromatic tetracyclic compounds is disclosed in the specification. The invention also provides a preparation method of the compounds and application of the compounds in preparation of antifungal drugs.

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