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34485-82-0

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34485-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34485-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,8 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34485-82:
(7*3)+(6*4)+(5*4)+(4*8)+(3*5)+(2*8)+(1*2)=130
130 % 10 = 0
So 34485-82-0 is a valid CAS Registry Number.

34485-82-0SDS

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 2-methyl-2-prop-1-en-2-yloxirane

1.2 Other means of identification

Product number -
Other names 2,3-dimethyl-1,3-butadiene monooxide

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:34485-82-0 SDS

34485-82-0Upstream product

34485-82-0Relevant articles and documents

Visible Light Induced Reactions of NO2 with Conjugated Dienes in a Low-Temperature Ar Matrix

Tanaka, Nobuaki,Kajii, Yoshizumi,Shibuya, Kazuhiko,Nakata, Munetaka

, p. 7048 - 7053 (1993)

Visible light induced oxygen atom transfer from NO2 to conjugated dienes has been investigated in a low-temperature Ar matrix, where the dienes are 1,3-butadiene (BD), 2-methyl-1,3-butadiene (isoprene), and 2,3-dimethyl-1,3-butadiene (DMB).In each diene/NO2/Ar system, the corresponding nitrite radical, oxirane, aldehyde, and NO were obtained as the photochemical reaction products.The reactions are initiated by the formation of undetecteable short-lived oxirane biradical and NO due to visible light induced O atom transfer from NO2 to the conjugated dienes. (1) The recombination of oxirane biradicals and neighboring NO gives the nitrite radicals as the photochemical intermediate. (2) The ring closure of the biradicals leads to the formation of oxiranes. (3) The intramolecular H atom transfer of biradicals leads to the formation of aldehydes.The visible photolysis of the nitrite radicals gives rise to oxirane, aldehyde, and NO.The reaction rates are derived by measuring the absorbance changes of the products upon the 582-nm irradiation.The methyl substituent effect on the reactivity is discussed.

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