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1129-92-6

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1129-92-6 Usage

Isomers

Mixture of cis (E) and trans (Z) isomers

Stereochemistry

(E,Z)designation indicates the arrangement of substituents on the double bond

E isomer

Substituents on the same side of the double bond

Z isomer

Substituents on opposite sides of the double bond

Applications

Precursor in the production of various industrial chemicals
Used in the synthesis of fragrance compounds
Employed in the production of synthetic resins
Utilized as additives in the rubber industry

Versatility

Wide range of applications in the chemical industry

Check Digit Verification of cas no

The CAS Registry Mumber 1129-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1129-92:
(6*1)+(5*1)+(4*2)+(3*9)+(2*9)+(1*2)=66
66 % 10 = 6
So 1129-92-6 is a valid CAS Registry Number.

1129-92-6SDS

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 cis,trans-1,3-cyclododecadiene

1.2 Other means of identification

Product number -
Other names .1Z,3E-Cyclododecadien

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:1129-92-6 SDS

1129-92-6Upstream product

1129-92-6Downstream Products

1129-92-6Relevant articles and documents

Isomerization of Cyclooctene and Cyclododecene Oxides Catalyzed by Solid Acids and Bases

Arata, Kazushi,Nakamura, Hideo,Nakamura, Yuki

, p. 2351 - 2353 (2007/10/02)

The title reactions were carried out over seven catalysts.From cyclooctene oxide a large amount of 7-octenal was formed together with 3-cycloocten-1-ol over SiO2-Al2O3 and SiO2-TiO2, 3-cycloocten-1-ol over solid H3PO4, and cyclooctanone over FeSO4.Most catalysts except for NiSO4, Al2O3, and Tio2-ZrO2 produced 1,3-cyclododecadiene, cyclododecanone, and 2-cyclododecen-1-ol uniformly from cyclododecene oxide.Allylic alcohols were preferentially given by Al2O3 and TiO2-ZrO2.

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