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116412-99-8

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116412-99-8 Usage

Uses

(3,4-Dimethoxyphenyl)(4-(trifluoromethyl)phenyl)methanone is a useful reagent in the preparation of benzophenones as fungicide intermediates.

Check Digit Verification of cas no

The CAS Registry Mumber 116412-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,1 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 116412-99:
(8*1)+(7*1)+(6*6)+(5*4)+(4*1)+(3*2)+(2*9)+(1*9)=108
108 % 10 = 8
So 116412-99-8 is a valid CAS Registry Number.

116412-99-8SDS

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 (3,4-dimethoxyphenyl)-[4-(trifluoromethyl)phenyl]methanone

1.2 Other means of identification

Product number -
Other names 4'-TRIFLUOROMETHYL-3,4-DIMETHOXYBENZOPHENONE

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:116412-99-8 SDS

116412-99-8Relevant articles and documents

Synthesis of two new naphthalene-containing compounds and their bindings to human serum albumin

Wang, Xia,Xing, Yue,Su, Jing,Wang, Changsheng,Wang, Zishi,Yu, Yinghui,Xu, Hongliang,Ma, DongSheng

, p. 3435 - 3448 (2020/07/04)

Two naphthalene-containing compounds, 4-hydroxy-6,7-dimethoxy-1-(4-(trifluoromethyl)phenyl)-2-naphthoic acid (A) and 4-hydroxy-6,7-dimethoxy-1-phenyl-2-naphthoic acid (B), were prepared by several steps. Their bindings to human serum albumin (HSA) were st

PHOTOCHROMIC MATERIALS DEMONSTRATING IMPROVED FADE RATES

-

Page/Page column 15, (2008/06/13)

Various photochromic materials are provided that are essentially free of polymerizable unsaturated groups, and comprise: a) an indeno[2′,3′:3,4]naphtho[1,2-b]pyran; and b) an electron-withdrawing, non-conjugating group bonded at the 11-position of the indeno[2′,3′:3,4]naphtho[1,2-b]pyran. Alternative embodiments include various substituents at other positions of the indeno[2′,3′:3,4]naphtho[1,2-b]pyran. Also provided are photochromic articles including a substrate and one of the above photochromic materials, in contact with at least a portion of the substrate.

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