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821-97-6

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821-97-6 Usage

General Description

(Z)-3-Undecene is a colorless liquid hydrocarbon with a molecular formula of C11H22. It is an unsaturated alkene compound with a double bond in the cis configuration, and it is commonly used as a chemical intermediate in the synthesis of various products such as fragrances, flavors, and polymers. (Z)-3-Undecene is known for its characteristic odor, and it is used in the manufacturing of perfumes and as a chemical building block in the production of specialty chemicals. It is also utilized in the production of insect pheromones and as a component in lubricant and fuel additives. Overall, (Z)-3-Undecene is a versatile chemical compound with various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 821-97-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 821-97:
(5*8)+(4*2)+(3*1)+(2*9)+(1*7)=76
76 % 10 = 6
So 821-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H22/c1-3-5-7-9-11-10-8-6-4-2/h5,7H,3-4,6,8-11H2,1-2H3/b7-5-

821-97-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-undec-3-ene

1.2 Other means of identification

Product number -
Other names undec-3c-ene

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:821-97-6 SDS

821-97-6Downstream Products

821-97-6Relevant articles and documents

The catalytic Shapiro reaction

Maruoka, Keiji,Oishi, Masataka,Yamamoto, Hisashi

, p. 2289 - 2290 (2007/10/03)

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HINDERED ORGANOBORON GROUPS IN ORGANIC SYNTHESIS. 14. STEREOSELECTIVE SYNTHESIS OF ALKENES BY THE BORON-WITTIG REACTION USING ALIPHATIC ALDEHYDES

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

, p. 5647 - 5650 (2007/10/02)

In the presence of HX, carbanions Mes2BCHLiR1 react with aliphatic aldehydes to give alkenes.The stereochemistry of product alkene depends upon the nature of HX.

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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