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Benzenemethanol, 4-hydroxy-a-(4-hydroxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69552-26-7

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69552-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69552-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,5 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69552-26:
(7*6)+(6*9)+(5*5)+(4*5)+(3*2)+(2*2)+(1*6)=157
157 % 10 = 7
So 69552-26-7 is a valid CAS Registry Number.

69552-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(4-hydroxyphenyl)methanol

1.2 Other means of identification

Product number -
Other names -

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:69552-26-7 SDS

69552-26-7Relevant academic research and scientific papers

Structural development of benzhydrol-type 1′-Acetoxychavicol Acetate (ACA) analogs as human leukemia cell-growth inhibitors based on Quantitative Structure-Activity Relationship (QSAR) analysis

Misawa, Takashi,Aoyama, Hiroshi,Furuyama, Taniyuki,Dodo, Kosuke,Sagawa, Morihiko,Miyachi, Hiroyuki,Kizaki, Masahiro,Hashimoto, Yuichi

experimental part, p. 1490 - 1495 (2009/10/01)

Benzhydrol-type analogs of 1′-acetoxychavicol acetate (ACA) were developed as inhibitors of human leukemia HL-60 cell growth based on quantitative structure-activity relationship (QSAR) analysis. An analog containing an anthracenyl moiety (8) was a potent inhibitor with the IC 50 value of 0.12 μM.

DEOXYGENATION OF ALDEHYDES AND KETONES WITH SODIUM CYANOBOROHYDRIDE

Elliger, Carl A.

, p. 1315 - 1324 (2007/10/02)

Treatment of hydroxy-substituted aromatic aldehydes and ketones with sodium cyanoborohydride yields the corresponding methylene compounds under conditions which favor intermediate carbonium ion formation.

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