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5129-73-7

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5129-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5129-73-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,2 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5129-73:
(6*5)+(5*1)+(4*2)+(3*9)+(2*7)+(1*3)=87
87 % 10 = 7
So 5129-73-7 is a valid CAS Registry Number.

5129-73-7SDS

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 N-propylbutanamide

1.2 Other means of identification

Product number -
Other names N-propylbutyramide

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:5129-73-7 SDS

5129-73-7Downstream Products

5129-73-7Relevant articles and documents

-

Vaughn,Sears

, p. 183,185 (1958)

-

Titanium cation-exchanged montmorillonite as an active heterogeneous catalyst for the Beckmann rearrangement under mild reaction conditions

Mitsudome, Takato,Matsuno, Tsuyoshi,Sueoka, Shoichiro,Mizugaki, Tomoo,Jitsukawa, Koichiro,Kaneda, Kiyotomi

supporting information, p. 5211 - 5214 (2012/11/07)

Titanium cation-exchanged montmorillonite acts as an efficient heterogeneous catalyst for the Beckmann rearrangement of a wide range of ketoximes including aromatic, aliphatic, and alicyclic ketoximes under mild reaction conditions. After the rearrangement reaction, titanium cation-exchanged montmorillonite is easily separated by simple filtration, and can be reused with retention of high efficiency.

TiCl4-Catalyzed Addition of HN3 to Aldehydes and Ketones. Thermolysis and Photolysis of α-Azido Ethers

Hassner, Alfred,Fibiger, Richard,Amarasekara, Ananda S.

, p. 22 - 27 (2007/10/02)

Aldehydes react with hydrazoic acid and alcohols in the presence of catalytic amounts of TiCl4 to produce α-azido ethers.The conversion of simple ketones to methyl α-azido alkyl ethers can be accomplished by means of hydrazoic acid and methyl orthoformate.Both gas-phase thermolysis and photolysis of representative α-azido ethers were studied and shown to produce mainly imino ethers.In the thermolysis, migratory preference decreases in the series H >> CH3 > Ph >> OR.

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