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176671-74-2

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176671-74-2 Usage

Chemical Properties

White Solid

Uses

[4-(PhenylMethoxy)phenyl][4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]-Methanone is used in the preparation of triarylethylenecarboxylic acids useful due to their estrogen receptor affinity and estrogenic potency.

Check Digit Verification of cas no

The CAS Registry Mumber 176671-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,6,7 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 176671-74:
(8*1)+(7*7)+(6*6)+(5*6)+(4*7)+(3*1)+(2*7)+(1*4)=172
172 % 10 = 2
So 176671-74-2 is a valid CAS Registry Number.

176671-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(Phenylmethoxy)phenyl][4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]-methanone

1.2 Other means of identification

Product number -
Other names [4-(oxan-2-yloxy)phenyl]-(4-phenylmethoxyphenyl)methanone

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:176671-74-2 SDS

176671-74-2Relevant articles and documents

Estrogen mimetics lacking reproductive tract effects

-

, (2008/06/13)

A method for treating symptoms, diseases and conditions in extra-reproductive tract tissues that are responsive to treatment with estrogen, using triarylethanes of formula (I) wherein R1is —O(CH2)mR3or —(CH2)nR3; wherein R3is an anionic substituent; m is an integer from 1 to 4; and n is an integer from 0 to 4; and wherein R2is either H or —OH. Each of R1and R2can be either meta or para to its respective phenyl ethyl linkage. Compounds having the formula (I) wherein R1is —O(CH2)mR3or —(CH2)nR3; R3is an anionic substituent; m is 1, 2, 3 or 4; n is 0, 1, 2, 3 or 4; R2is H or —OH; and wherein each of R1and R2is independently meta or para to its respective phenyl ethyl linkage are also provided, with the proviso that R2is not para —OH when m is 1 and R3is —COOH.

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