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2783-10-0

5-Methyl-1,3-hexadiene is an organic compound with the molecular formula C7H12. It is a colorless liquid with a strong, pungent odor. This unsaturated hydrocarbon is a member of the diene class, which means it contains two carbon-carbon double bonds. The structure of 5-methyl-1,3-hexadiene consists of a six-carbon chain with a methyl group attached to the fifth carbon and double bonds between the first and second, as well as the third and fourth carbon atoms. It is used as a chemical intermediate in the synthesis of various organic compounds, such as fragrances, pharmaceuticals, and polymers. Due to its reactive nature, it is important to handle 5-methyl-1,3-hexadiene with care, as it can be flammable and may cause irritation to the skin, eyes, and respiratory system.

2783-10-0

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2783-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2783-10-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,8 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2783-10:
(6*2)+(5*7)+(4*8)+(3*3)+(2*1)+(1*0)=90
90 % 10 = 0
So 2783-10-0 is a valid CAS Registry Number.

2783-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-METHYL-1,3-HEXADIENE

1.2 Other means of identification

Product number -
Other names 5-Methyl-5-hexenoic acid

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:2783-10-0 SDS

2783-10-0Relevant articles and documents

Regio- and Stereoselective Hydrosulfonylation of Conjugated Dienes via a (?-Allyl)palladium Complex

Tamaru, Yoshinao,Yamada, Yoshimi,Kagotani, Masahiro,Ochiai, Hirofumi,Nakajo, Eiji,et al.

, p. 4669 - 4681 (2007/10/02)

The combination of a sulfonylpalladation of acyclic dienes 1 (with 2 equiv of NaSO2R and 1 equiv of PdCl2 in acetic acid or acetic acid-H2O at 50-80 deg C under air) and a protiodepalladation of the thus obtained palladium complexes 3 with dimethylglyoxime (in a protic solvent at room temperature) provides di- and trisubstituted (Z)-Δ3-sulfones 12 selectively, irrespective of the stereochemistry of the starting dienes.Similar treatment of 1-vinylcycloalkenes 5 (n (1,3) strain between Pd and the substituent on the allylic position.

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