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(Z)-1-phenyl-2-propyl-3-(p-tolyl)hex-2-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1043871-06-2

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1043871-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1043871-06-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,3,8,7 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1043871-06:
(9*1)+(8*0)+(7*4)+(6*3)+(5*8)+(4*7)+(3*1)+(2*0)+(1*6)=132
132 % 10 = 2
So 1043871-06-2 is a valid CAS Registry Number.

1043871-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-1-phenyl-2-propyl-3-(p-tolyl)hex-2-en-1-ol

1.2 Other means of identification

Product number -
Other names 2Z-1-phenyl-2-propyl-3-p-tolylhex-2-en-1-ol

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:1043871-06-2 SDS

1043871-06-2Relevant academic research and scientific papers

A facile Zr-mediated multicomponent approach to arylated allylic alcohols and its application to the synthesis of highly substituted indenes and spiroindenes

Guo, Shenghai,Liu, Yuanhong

experimental part, p. 2064 - 2070 (2009/02/01)

An efficient and one-pot procedure for the synthesis of arylated and stereodefined allylic alcohols has been achieved through zirconium-mediated multicomponent coupling reactions of alkynes, aldehydes (or ketones), and aryl iodides. The subsequent intramo

Alkynes as activators in the nickel-catalysed addition of organoboronates to aldehydes

Takahashi, Go,Shirakawa, Eiji,Tsuchimoto, Teruhisa,Kawakami, Yusuke

, p. 1459 - 1461 (2007/10/03)

Alkynes act not as substrates but as co-catalysts in the presence of a nickel catalyst, an organoboronate and an aldehyde to promote the addition reaction between the substrates in combination with H2O. The Royal Society of Chemistry 2005.

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