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10264-17-2

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10264-17-2 Usage

General Description

N-Hexylbutyramide is a chemical compound with the molecular formula C10H21NO2. It is an amide derivative of butyric acid, with a six-carbon hexyl group attached to the nitrogen atom. N-Hexylbutyramide is commonly used as a flavoring agent in food products and as a fragrance ingredient in perfumes and cosmetics. It is also utilized in the production of pharmaceuticals and as a solvent in various industrial applications. N-Hexylbutyramide has a mild, fruity odor and is classified as a low-to-moderate hazard substance, with limited toxicological data available. Overall, N-Hexylbutyramide has various practical uses and applications with a relatively low risk profile.

Check Digit Verification of cas no

The CAS Registry Mumber 10264-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,6 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10264-17:
(7*1)+(6*0)+(5*2)+(4*6)+(3*4)+(2*1)+(1*7)=62
62 % 10 = 2
So 10264-17-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H21NO/c1-3-5-6-7-9-11-10(12)8-4-2/h3-9H2,1-2H3,(H,11,12)

10264-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name N-hexylbutanamide

1.2 Other means of identification

Product number -
Other names Butanamide,N-hexyl

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:10264-17-2 SDS

10264-17-2Downstream Products

10264-17-2Relevant articles and documents

Functionalisation of aldehydes via aerobic hydroacylation of azodicarboxylates 'on' water

Chudasama, Vijay,Ahern, Jenna M.,Dhokia, Dipti V.,Fitzmaurice, Richard J.,Caddick, Stephen

, p. 3269 - 3271 (2011)

Herein we report the functionalisation of aldehydes via hydroacylation of azodicarboxylates. A range of functionalised aldehydes are employed as the limiting reagent including chiral non-racemic aldehydes bearing α-stereocentres which are functionalised giving access to enantiomerically pure products. The resultant hydrazides can be employed as acyl donors in the synthesis of amides.

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