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3-Heptene, 6-methyl-, also known as 6-methyl-3-heptene, is an organic compound with the molecular formula C8H16. It is a colorless liquid with a strong, pungent odor. This alkene is a member of the heptene family, which consists of seven carbon atoms in a linear chain, with a double bond between the third and fourth carbon atoms. The 6-methyl-3-heptene specifically has a methyl group (CH3) attached to the sixth carbon atom in the chain. It is used as a chemical intermediate in the synthesis of various organic compounds, such as fragrances, pharmaceuticals, and other specialty chemicals. Due to its reactive nature, it is essential to handle 6-methyl-3-heptene with proper safety precautions to avoid potential health and environmental risks.

3404-57-7

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3404-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3404-57-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3404-57:
(6*3)+(5*4)+(4*0)+(3*4)+(2*5)+(1*7)=67
67 % 10 = 7
So 3404-57-7 is a valid CAS Registry Number.

3404-57-7Relevant academic research and scientific papers

Zirconium porphyrins as novel active catalysts for highly regio- And stereoselective ethylalumination of alkynes

Shibata, Kenji,Aida, Takuzo,Inoue, Shohei

, p. 1077 - 1080 (2007/10/02)

Zirconium(IV) complexes of 5, 10, 15, 20-tetraphenylporphyrin ((TPP)ZrX2) catalyze highly regioand stereo-selective ethylalumination of terminal alkynes with satisfactorily high turnover numbers.

A NEW STRATEGY FOR THE STEREOSELECTIVE SYNTHESIS OF OLEFINS

Dybowski, Piotr,Skowronska, Aleksandra

, p. 4385 - 4388 (2007/10/02)

Highly stereoselective conversion of ketones into (Z)-olefins, via intermediate S-(β-oxoalkyl)thiophosphates and their seleno analogues is described.

Synthesis of Olefins from α-Chlorocarbonyl Compounds

Barluenga, Jose,Yus, Miguel,Concellon, Jose M.,Bernad, Pablo

, p. 677 - 692 (2007/10/02)

Olefins or diolefins with the double bonds in predetermined positions are obtained in moderate to good yields by treatment of α-chlorocarbonyl compounds with Grignard reagents and lithium in a single process.

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