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7476-12-2

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7476-12-2 Usage

Physical state

White crystalline solid

Texture

Powdery

Odor

Sweet floral

Uses

a. Fragrance ingredient in perfumes, cosmetics, and personal care products
b. UV filter in sunscreens to protect skin from harmful UV radiation
c. Photoinitiator in the production of polymers
d. Chemical intermediate in the synthesis of various compounds

Acute toxicity

Low

Prolonged exposure effects

Can cause irritation to skin and eyes

Check Digit Verification of cas no

The CAS Registry Mumber 7476-12-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7476-12:
(6*7)+(5*4)+(4*7)+(3*6)+(2*1)+(1*2)=112
112 % 10 = 2
So 7476-12-2 is a valid CAS Registry Number.

7476-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,3-tetraphenylpropan-1-one

1.2 Other means of identification

Product number -
Other names phenyl 1,3,3-triphenylprop-2-enyl ketone

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:7476-12-2 SDS

7476-12-2Relevant articles and documents

Arylboronic Acid Catalyzed Dehydrative Mono-/Dialkylation Reactions of β-Ketoacids and Alcohols

Feng, Juhua,Hu, Haipeng,Ni, Hailiang,Qiu, Yuqian,Wang, Cuilin,Wang, Guangtu,Wang, Hanguang,Wang, Wei,Wu, Xin,Yue, Guizhou,Zou, Ping

supporting information, p. 832 - 836 (2022/02/05)

The dehydrative mono-/dialkylation reactions of alcohols and β-ketoacids were realized under arylboronic acid catalysis, furnishing a series of β-aryl ketones and β-ketoesters in yields of 15–99%, with CO2 and H2O being the byproduct

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