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Z-7-decen-2-ol, also known as cis-7-decen-2-ol, is a colorless liquid with a strong, fatty, and green odor. It is an organic compound belonging to the class of alkenols, characterized by the presence of a double bond between the 7th and 8th carbon atoms in a decane chain, with a hydroxyl group attached to the 2nd carbon. This chemical is widely used in the fragrance industry as a component in various perfumes, soaps, and cosmetics due to its ability to mimic natural green and fruity scents. It is also employed in the food industry as a flavoring agent, particularly in the creation of artificial fruit flavors. Z-7-decen-2-ol is synthesized through various chemical processes, and its safety profile is generally considered to be low risk when used in accordance with recommended guidelines.

81980-06-5

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81980-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81980-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,9,8 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81980-06:
(7*8)+(6*1)+(5*9)+(4*8)+(3*0)+(2*0)+(1*6)=145
145 % 10 = 5
So 81980-06-5 is a valid CAS Registry Number.

81980-06-5Downstream Products

81980-06-5Relevant academic research and scientific papers

Alkylaluminum Halide Induced Cyclization of Unsaturated Carbonyl Compounds

Snider, Barry B.,Karras, Michael,Price, Robert T.,Rodini, David J.

, p. 4538 - 4545 (2007/10/02)

2,6-Dimethyl-5-heptenal (3) and 5-octenal (24) undergo concerted ene reactions with 1 equiv of Me2AlCl and cation-olefin cyclizations with 2 equiv of Me2AlCl, MeAlCl2, or EtAlCl2 to give a zwitterion which reacts to give several products including an ene

ALKYLALUMINIUM HALIDES; LEWIS ACID CATALYSTS WHICH ARE BRONSTED BASES

Snider, Barry B.,Rodini, David J.,Karras, Michael,Kirk, Thomas C.,Deutsch, Ethan A.,et al.

, p. 3927 - 3934 (2007/10/02)

Alkylaluminium halides react with Broensted acids to liberate an alkane and generate a new Lewis acid.Using these reagents, Lewis acid catalyzed reactions can be run under aprotic conditions, even when acidic protons are produced in the reaction.The use of these reagents for Lewis acid catalyzed ene, Diels-Alder and cycloaddition reactions and Claisen rearrangements is described.These reagents are also useful initiators for cation-olefin addition reactions.In some cases the alkyl groups react as nucleophiles.While this is often undesirable, addition of an alkyl group to carbenium ion intermediates provides novel classes of compounds.

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