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1-Isobutyl-1-cyclohexene is an organic compound with the molecular formula C??H??. It is a cyclic alkene with a cyclohexane ring and an isobutyl group attached to one of the carbon atoms in the ring. 1-Isobutyl-1-cyclohexene is characterized by its unique structure, which consists of a six-membered carbon ring with alternating single and double bonds, and a three-carbon isobutyl chain branching off from one of the ring's carbon atoms. 1-Isobutyl-1-cyclohexene is a colorless liquid with a pungent odor and is insoluble in water. It is used in the synthesis of various chemicals, pharmaceuticals, and fragrances due to its reactive double bond and unique structural features.

3983-03-7

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3983-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3983-03-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,8 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3983-03:
(6*3)+(5*9)+(4*8)+(3*3)+(2*0)+(1*3)=107
107 % 10 = 7
So 3983-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H18/c1-9(2)8-10-6-4-3-5-7-10/h6,9H,3-5,7-8H2,1-2H3

3983-03-7Relevant academic research and scientific papers

ORGANIC COMPOUNDS

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Page/Page column 5, (2009/01/24)

The present invention relates to 1-(2-isobutylcyclohex-1-enyl)but-2-en-1-one and 1-(2-isobutylcyclohex-2-enyl)but-2-en-1-one and their use as fragrance ingredient.

PERFUME SYSTEMS

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, (2009/01/20)

The present application relates to perfume systems and consumer products comprising new perfumes and/or such perfume systems, as well as processes for making and using such perfume systems and consumer products.

Enantioselective protonation of samarium enolates derived from α- heterosubstituted ketones and lactone by SmI2-mediated reduction

Nakamura, Yutaka,Takeuchi, Seiji,Ohgo, Yoshiaki,Yamaoka, Makoto,Yoshida, Akihiro,Mikami, Koichi

, p. 4595 - 4620 (2007/10/03)

SmI2-mediated reductive cleavage of α-heterosubstituents of α-alkyl or α-aryl ketones and lactone gave the corresponding 'thermodynamic samarium enolates'. Enantioselective protonation of the samarium enolates with C2- symmetric chiral diols afforded the corresponding ketones and lactone in moderate to high enantioselectivities.

The Reaction of Organoboranes with Lithium Salts of Trisylhydrazones of Cycloalkanones Followed by Treatment with Iodine

Baba, Tsutomu,Avasthi, Kamlakar,Suzuki, Akira

, p. 1571 - 1572 (2007/10/02)

The titled reaction proceeds smoothly under mild conditions to give corresponding 1-alkylcycloalkenes in excellent yields.The overall reaction provides a convenient synthetic procedure of cycloalkenes for cycloalkanones, with various alkyl substituents readily available by means of hydroboration.

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