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1,5-endoperoxy-2-hydroperoxycarot-3-ene-4-carbaldehyd is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133303-03-4

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133303-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133303-03-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,0 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133303-03:
(8*1)+(7*3)+(6*3)+(5*3)+(4*0)+(3*3)+(2*0)+(1*3)=74
74 % 10 = 4
So 133303-03-4 is a valid CAS Registry Number.

133303-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-endoperoxy-2-hydroperoxycarot-3-ene-4-carbaldehyd

1.2 Other means of identification

Product number -
Other names 1,5-epidioxy-2-hydroperoxycarot-3-en-14-al

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:133303-03-4 SDS

133303-03-4Downstream Products

133303-03-4Relevant academic research and scientific papers

Identification of an Intermediate in Autoxidation of Carota-1,4-dien-14-al into Rugosal A

Hashidoko, Yasuyuki,Tahara, Satoshi,Mizutani, Junya

, p. 211 - 214 (2007/10/02)

In the autoxidation of (7R,10R)-carota-1,4-dien-14-al 1, which is a precursor of an antifungal compound rugosal A 2, in Rosa rugosa leaves, an intermediate possessing a 1,5-endoperoxy-2-hydroperoxy system 4 was isolated as a major product.The structures of compound 4 and other by-products including rugosal A 2 and rugosic acid A 3 were determined.These autoxidation products indicated the conversion pathway of compound 1 into rugosal A 2, similar to the radical reaction pathway in the autoxidation of polyunsaturated fatty acids.

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