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7256-14-6

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7256-14-6 Usage

General Description

2,3,4,5,6-pentahydroxyhexanamide, also known as a non-preferred name, is an organic compound with the molecular formula C6H13NO6. It is a derivative of hexane and contains a primary amide functional group. 2,3,4,5,6-pentahydroxyhexanamide (non-preferred name) is a white solid at room temperature and is soluble in water. It has five hydroxyl groups attached to a six-carbon chain and an amide group, making it a complex molecule with multiple potential hydrogen bonding sites. Its specific chemical properties and potential applications are determined by its structural features, and it may have uses in fields such as pharmaceuticals, food additives, or organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 7256-14-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7256-14:
(6*7)+(5*2)+(4*5)+(3*6)+(2*1)+(1*4)=96
96 % 10 = 6
So 7256-14-6 is a valid CAS Registry Number.

7256-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,5,6-pentahydroxyhexanamide

1.2 Other means of identification

Product number -
Other names GALACTONO-1,4-LACTONE,D

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:7256-14-6 SDS

7256-14-6Relevant articles and documents

Direct oxidative amidation of aldoses by iodine in ammonia water

Chen, Ming-Yi,Hsu, Jue-Liang,Shie, Jiun-Jie,Fang, Jim-Min

, p. 129 - 133 (2007/10/03)

Aldopentoses, aldohexoses and the benzylated derivatives reacted with iodine in ammonia water at room temperature to give their corresponding saccharide amides in high yields. The reactions proceeded with oxidation of the aldose hemiacetals by iodine to g

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