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470-14-4

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470-14-4 Usage

General Description

2-Pentanone, 1,3,4,5-tetrahydroxy-4-(hydroxymethyl)- is a compound that contains a ketone group and four hydroxyl groups. Its chemical formula is C5H12O5 and it is commonly used in the synthesis of organic compounds and pharmaceuticals. This chemical is a colorless, highly reactive compound that is soluble in water and other organic solvents. It is also known for its ability to act as a chelating agent, forming complexes with metal ions. Due to its unique chemical structure, it has a variety of potential applications in the fields of medicine, chemical engineering, and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 470-14-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 470-14:
(5*4)+(4*7)+(3*0)+(2*1)+(1*4)=54
54 % 10 = 4
So 470-14-4 is a valid CAS Registry Number.

470-14-4SDS

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 1,3,4,5-tetrahydroxy-4-(hydroxymethyl)pentan-2-one

1.2 Other means of identification

Product number -
Other names 1,3,4,5-Tetrahydroxy-4-hydroxymethyl-pentan-2-on

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:470-14-4 SDS

470-14-4Relevant articles and documents

Aldol type reaction of unprotected sugars in methanol

Saimoto, Hiroyuki,Yatani, Setsuo,Sashiwa, Hitoshi,Shigemasa, Yoshihiro

, p. 937 - 938 (2007/10/02)

Although aldol condensation of 1,3-dihydroxyacetone with formaldehyde in methanol catalyzed by CaCl2/KOH gave glycero-tetrulose, the reaction catalyzed by Ca(OH)2 preferentially gave 1,3-dihydroxyacetone dimer. The result was explained by the formation of a chelated enolate. This sequence was successfully applied to the stereoselective synthesis of threo-3-pentulose.

Analysis, by g. l. c. - m. s. after isopropylidenation, of the product mixtures obtained by aldol condensation of glycolaldehyde and 1,3-dihydroxy-2-propanone

Morgenlie, Svein

, p. 330 - 334 (2007/10/02)

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