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3-Methyl-1,4,6-heptatriene is an organic compound with the molecular formula C8H12. It is a conjugated diene, which means it has a chain of alternating double and single bonds, with a methyl group attached to the third carbon atom. 3-METHYL-1,4,6-HEPTATRIENE is a colorless liquid with a strong, pungent odor. It is insoluble in water but soluble in organic solvents such as ethanol and ether. 3-Methyl-1,4,6-heptatriene is used as a chemical intermediate in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and fragrances. It is also used as a reagent in organic chemistry for various reactions, such as Diels-Alder reactions. Due to its reactive nature, it should be handled with care and stored in a cool, dry place away from heat and open flames.

925-52-0

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925-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 925-52-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 925-52:
(5*9)+(4*2)+(3*5)+(2*5)+(1*2)=80
80 % 10 = 0
So 925-52-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H12/c1-4-6-7-8(3)5-2/h4-8H,1-2H2,3H3/b7-6+

925-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-1,3,6-Heptatriene

1.2 Other means of identification

Product number -
Other names 1,3,6-Heptatriene, 5-methyl-

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:925-52-0 SDS

925-52-0Downstream Products

925-52-0Relevant academic research and scientific papers

Co-catalyzed cross-coupling of alkyl halides with tertiary alkyl Grignard reagents using a 1,3-butadiene additive

Iwasaki, Takanori,Takagawa, Hiroaki,Singh, Surya P.,Kuniyasu, Hitoshi,Kambe, Nobuaki

supporting information, p. 9604 - 9607 (2013/07/26)

The cobalt-catalyzed cross-coupling of alkyl (pseudo)halides with alkyl Grignard reagents in the presence of 1,3-butadiene as a ligand precursor and LiI is described. Sterically congested quaternary carbon centers could be constructed by using tertiary alkyl Grignard reagents. This reaction proceeds via an ionic mechanism with inversion of stereochemistry at the reacting site of the alkyl halide and is compatible with various functional groups. The use of both 1,3-butadiene and LiI was essential for achieving high yields and high selectivities.

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