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Benzenemethanol, a-(1-methyl-3-butynyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89110-89-4

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89110-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89110-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,1 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89110-89:
(7*8)+(6*9)+(5*1)+(4*1)+(3*0)+(2*8)+(1*9)=144
144 % 10 = 4
So 89110-89-4 is a valid CAS Registry Number.

89110-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-1-phenyl-4-pentyn-1-ol

1.2 Other means of identification

Product number -
Other names 2-Methyl-1-phenyl-pent-4-yn-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:89110-89-4 SDS

89110-89-4Relevant academic research and scientific papers

Lewis acid catalyzed stereoselective hydrosilylation of ketones under the control of σ-π chelation

Asao, Naoki,Ohishi, Takeshi,Sato, Kenichiro,Yamamoto, Yoshinori

, p. 8195 - 8203 (2007/10/03)

Hydrosilylation of 2-methyl-1-phenyl-pentan-1-one with Et3SiH in the presence of catalytic amounts of B(C6F5)3 gave the anti-product with slight predominance over syn-product (syn/anti=1:1.5). In contrast, the s

A RING OPENING REACTION OF OXETANES WITH LITHIUM ACETYLIDES PROMOTED BY BORON TRIFLUORIDE ETHERATE

Yamaguchi, Masahiko,Nobayashi, Yukio,Hirao, Ichiro

, p. 4261 - 4266 (2007/10/02)

Several substituted oxetanes were treated with lithium acetylides in the presence of boron trifluoride etherate to give γ-hydroxyacetylenes.The reaction conditions were varied and several synthetic features of the present reaction were revealed.

THE ALKYNYLATION REACTION OF OXETHANES

Yamaguchi, Masahiko,Nobayashi, Yukio,Hirao, Ichiro

, p. 5121 - 5122 (2007/10/02)

γ-Hydroxyacetylenes were synthesized in high yields by the reaction of oxetanes with lithium acetylides in the presence of boron trifluoride etherate.

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