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53398-76-8

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53398-76-8 Usage

General Description

2,4-Hexadienal is a chemical compound that belongs to the class of aldehydes. It is a colorless liquid with a pungent odor and is found naturally in various plants and fruits. It is commonly used as a flavoring and fragrance agent in the food and cosmetic industries. In addition, it is also used in the production of perfumes and as a chemical intermediate in the synthesis of other compounds. However, 2,4-Hexadienal poses certain health hazards and precautions should be taken when handling and using this chemical. It is important to use proper protective equipment and follow safety guidelines when working with 2,4-Hexadienal to minimize the risk of exposure and potential health effects.

Check Digit Verification of cas no

The CAS Registry Mumber 53398-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,9 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53398-76:
(7*5)+(6*3)+(5*3)+(4*9)+(3*8)+(2*7)+(1*6)=148
148 % 10 = 8
So 53398-76-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O/c1-2-3-4-5-6-7/h2-6H,1H3/b3-2-,5-4+

53398-76-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E,4Z)-hexa-2,4-dien-1-al

1.2 Other means of identification

Product number -
Other names (2E,4Z)-2,4-hexadienal

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:53398-76-8 SDS

53398-76-8Relevant articles and documents

Total synthesis of sperabillin A and C

Allmendinger, Lars,Bauschke, Gerd,Paintner, Franz F.

, p. 2615 - 2618 (2007/10/03)

The first total synthesis of sperabillin A and an improved total synthesis of sperabillin C have been achieved in 11 steps from N-Boc-Omethyl-L-tyrosine. The stereoselective pathway to the core (3R,5R)-3,6-diamino-5-hydroxyhexanoic acid involves an Arndt-

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