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Benzene, (4-ethenyl-4,8-dimethyl-1,7-nonadienyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92511-60-9

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92511-60-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92511-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,1 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92511-60:
(7*9)+(6*2)+(5*5)+(4*1)+(3*1)+(2*6)+(1*0)=119
119 % 10 = 9
So 92511-60-9 is a valid CAS Registry Number.

92511-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-4,8-dimethyl-1-phenyl-4-vinylnona-1,7-diene

1.2 Other means of identification

Product number -
Other names ((E)-4,8-Dimethyl-4-vinyl-nona-1,7-dienyl)-benzene

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:92511-60-9 SDS

92511-60-9Downstream Products

92511-60-9Relevant academic research and scientific papers

Regioselective Head-to-tail Coupling of Allylic Trialkylstannanes with Allylic Halides under High Pressure

Yamamoto, Yoshinori,Maruyama, Kazuhiro,Matsumoto, Kiyoshi

, p. 548 - 549 (1984)

Allylic trialkylstannanes (1) regioselectively react with allylic halides (2) at room temperature under high pressure (10 kbar) to give head-to-tail coupling products (3) in high yields.

Selective Alkylation and Allylation of Allylic Halides by Tetraorganoidates: Regio- and Stereo-selective Synthesis of Rosefuran and Sesquirosefuran

Araki, Shuki,Jin, Shun-Ji,Butsugan, Yasuo

, p. 549 - 552 (2007/10/02)

Tetraalkylindanes regioselectively alkylate allylic bromides at the α-carbon.In this way, 1,5-dienes have been regio- and stereo-selectively synthesized by the allyl-allyl coupling of allylic bromides and allylic indates, including rosefuran 1 and sequirosefuran 3.

Application of Indium Ate Complexes to Synthetic Chemistry. Selective Conjugate Addition to Enones and Coupling with Allylic Halides

Araki, Shuki,Shimizu, Toshio,Jin, Shun-Ji,Butsugan, Yasuo

, p. 824 - 825 (2007/10/02)

Tetraorganoindium ate complexes, prepared by the addition of organolithium reagents to trialkylindium, reacted with α,β-unsaturated ketones in a 1,4-addition fashion; allylic indates derived from allylic indium sesquihalides coupled with allylic halides regio- and stereo-specifically to give high yields of hed-to-tail 1,5-dienes.

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