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2-bromo-N,N-dipropan-2-yl-propanamide is a chemical compound with the molecular formula C9H18BrNO. It is a derivative of propanamide, featuring a bromine atom at the 2-position and two propyl groups attached to the nitrogen atom. This organic compound is characterized by its unique structure, which includes a carbonyl group (C=O) and an amide linkage. It is a colorless liquid with a relatively high boiling point and is soluble in organic solvents. Due to its specific functional groups and molecular structure, 2-bromo-N,N-dipropan-2-yl-propanamide has potential applications in various chemical reactions and synthesis processes, such as the formation of pharmaceuticals, agrochemicals, and other specialty chemicals.

5327-04-8

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5327-04-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5327-04-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5327-04:
(6*5)+(5*3)+(4*2)+(3*7)+(2*0)+(1*4)=78
78 % 10 = 8
So 5327-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H18BrNO/c1-6(2)11(7(3)4)9(12)8(5)10/h6-8H,1-5H3

5327-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-N,N-di(propan-2-yl)propanamide

1.2 Other means of identification

Product number -
Other names 2-BROMO-N,N-DIPROPAN-2-YL-PROPANAMIDE

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:5327-04-8 SDS

5327-04-8Relevant academic research and scientific papers

Diastereodivergency in the reactions of 3-metallated-2-methylbutanamide

Asaoka, Morio,Tanaka, Michiko,Houkawa, Takashi,Ueda, Tsuyoshi,Sakami, Satoshi,Takei, Hisashi

, p. 471 - 486 (2007/10/03)

Diastereocontrolled reactions with 3-iodozinc-2-methylbutanamide were examined. When the iodozinc reagent was reacted with aromatic and α,β- unsaturated aldehydes in the presence of iodotrimethylsilane, C2-C3 anti- derivatives were obtained almost exclusively. Whereas, after transmetallation to Ti(IV), the reaction with aldehydes gave C2-C3 syn-derivatives exclusively. Acylation of the zinc reagent with acid chlorides in the presence of Pd(0) catalyst gave C2-C3 syn-derivatives.

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