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94723-93-0

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94723-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94723-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,7,2 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 94723-93:
(7*9)+(6*4)+(5*7)+(4*2)+(3*3)+(2*9)+(1*3)=160
160 % 10 = 0
So 94723-93-0 is a valid CAS Registry Number.

94723-93-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid (E)-4-(3-hydroxypropenyl)phenyl ester

1.2 Other means of identification

Product number -
Other names 4-((E)-3-hydroxyprop-1-enyl)phenyl acetate

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:94723-93-0 SDS

94723-93-0Relevant articles and documents

MELANIN GENERATION INHIBITOR AND WHITENING AGENT

-

Paragraph 0078; 0079, (2017/04/20)

PROBLEM TO BE SOLVED: To provide a melanin generation inhibitor and a whitening agent that are excellent in whitening effect and also excellent in safety and temporal stability. SOLUTION: The invention provides a melanin generation inhibitor containing a compound represented by formula [1] as an active ingredient, a whitening agent, as well as a melanin generation inhibiting method and a whitening method by applying such agents to the skin. (R1, R2, R4, and R5 are each independently H, a hydroxyl group, an alkyl group of C1-4, or -O-C(=O)R6; R6 is an alkyl group of C1-4; R3 is H, an alkyl group of C1-4, or -C(=O)R7; and R7 is an alkyl group of C1-8.) SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Enantioselective synthesis of (-)-cytoxazone and (+)-epi-cytoxazone, novel cytokine modulators via Sharpless asymmetric epoxidation and l-proline catalyzed Mannich reaction

Paraskar, Abhimanyu S.,Sudalai, Arumugam

, p. 5756 - 5762 (2007/10/03)

A short and efficient enantioselective synthesis of (-)-cytoxazone and its stereoisomer (+)-epi-cytoxazone, novel cytokine modulators, has been described with good yield and enantioselectivity. Ti-catalyzed Sharpless asymmetric epoxidation of allyl alcoho

A mild synthesis of coumaryl, coniferyl, sinapyl aldehydes and alcohols

Daubresse,Francesch,Mhamdi,Rolando

, p. 369 - 371 (2007/10/02)

Acetylconiferyl aldehyde is obtained from acetylvanillin by a Wittig reaction under phase-transfer conditions; basic hydrolysis gives coniferyl aldehyde, or after reduction with sodium borohydride affords coniferyl alcohol. This method is extended to the sinapyl and coumaryl series.

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