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1002-68-2

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1002-68-2 Usage

General Description

(E)-3-Undecene is a colorless liquid hydrocarbon with the molecular formula C11H22. It is a linear alpha olefin that is commonly used as a chemical intermediate in the manufacture of various products, including perfumes, flavors, and other organic compounds. (E)-3-Undecene is known for its pleasant, sweet, and floral odor, making it a popular ingredient in the fragrance industry. It is also utilized in the production of detergents, lubricants, and plasticizers, as well as in the synthesis of other chemicals. Additionally, (E)-3-Undecene has applications in the field of organic synthesis and is used as a reactant in various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 1002-68-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1002-68:
(6*1)+(5*0)+(4*0)+(3*2)+(2*6)+(1*8)=32
32 % 10 = 2
So 1002-68-2 is a valid CAS Registry Number.

1002-68-2Downstream Products

1002-68-2Relevant articles and documents

HINDERED ORGANOBORON GROUPS IN ORGANIC SYNTHESIS. 13. THE DIRECT PRODUCTION OF KETONES FROM ALIPHATIC ALDEHYDES BY A UNIQUE VARIANT OF THE BORON-WITTIG REACTION

Pelter, Andrew,Smith, Keith,Elgendy, Said,Rowlands, Martin

, p. 5643 - 5646 (1989)

In the presence of trifluoroacetic anhydride or N-chlorosuccinimide, aliphatic aldehydes react with dimesitylboron stabilised carbanions to give after work up, the corresponding ketones, a process wich is unique among Wittig type reactions.Yields of ketones are satisfactory in all cases except those involving the anion derived from the parent compound dimesitylmethylborane, wich give the corresponding alkenes.

TRANSITION METHAL-CATALYZED SUBSTITUTION REACTION OF ALLYLIC PHOSPHATES WITH GRIGNARD REAGENTS

Yanagisawa, Akira,Nomura, Nobuyoshi,Yamamoto, Hisashi

, p. 6017 - 6028 (2007/10/02)

SN2-selective Grignard coupling with primary allylic diphenylphosphates was successfully achieved using Ni or Fe catalyst.In sharp contrast, a catalytic amount of CuCN*2LiCl promoted a SN2'-selective coupling reaction.In the presence of the copper catalyst, stereochemically homogeneous γ-disubstituted allyl Grignard reagents reacted at the less substituted allylic terminus (α-position) with an allylic diphenylphosphate selectively without losing the double bond geometry.

DECARBOXYLATION OF ALIPHATIC α,β-UNSATURATED ALDEHYDES USING THE WILKINSON COMPLEX

Grigor'eva, N. Ya.,Pinsker, O. A.,Semenovskii, A. V.

, p. 593 - 594 (2007/10/02)

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