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5614-78-8

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5614-78-8 Usage

General Description

6-Chromanol is a chemical compound belonging to the chromanol group, which is known for its antioxidant properties. It is often used as an additive in cosmetics and skincare products due to its ability to protect the skin from damage caused by free radicals. Additionally, 6-Chromanol has been studied for its potential benefits in preventing oxidative stress and inflammation, which are linked to various health conditions such as heart disease and aging. Its antioxidant properties make it a valuable ingredient in a wide range of products aimed at promoting skin health and overall well-being.

Check Digit Verification of cas no

The CAS Registry Mumber 5614-78-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,1 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5614-78:
(6*5)+(5*6)+(4*1)+(3*4)+(2*7)+(1*8)=98
98 % 10 = 8
So 5614-78-8 is a valid CAS Registry Number.

5614-78-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dihydro-2H-chromen-6-ol

1.2 Other means of identification

Product number -
Other names 3,4-dihydro-6-hydroxy-2H-1-benzopyran

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:5614-78-8 SDS

5614-78-8Downstream Products

5614-78-8Relevant articles and documents

An efficient multigram-scale synthesis of 4-(ω-chloroalkoxy)phenols

Zinin,Stepanova,Jost,Kondakov,Shpirt,Chizhov,Torgov,Kononov

, p. 304 - 312 (2017/07/11)

Efficient multigram two-step syntheses of 4-(2-chloroethoxy)phenol and 4-(3-chloropropoxy)phenol in >70% yields starting from 4-hydroxybenzaldehyde and reagents with general formula Cl(CH2)nX (X = Cl, n = 2; X = OTs, n = 3) are proposed. 4-(2-Chloroethoxy)phenol can also be conveniently prepared from 4-methoxyphenol and 1,2-dichloroethane. The compounds thus obtained can be used in carbohydrate chemistry to synthesize glycosides bearing "universal" 4-(ω-chloroalkoxy)phenyl aglycons.

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