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16709-34-5

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16709-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16709-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,0 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16709-34:
(7*1)+(6*6)+(5*7)+(4*0)+(3*9)+(2*3)+(1*4)=115
115 % 10 = 5
So 16709-34-5 is a valid CAS Registry Number.

16709-34-5SDS

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 5-deoxy-D-threo-pent-2-ulose 1-phosphate

1.2 Other means of identification

Product number -
Other names Dg-threo-3,4-Dihydroxy-1-phosphonooxy-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:16709-34-5 SDS

16709-34-5Relevant articles and documents

Activated αβ-unsaturated aldehydes as substrate of dihydroxyacetone phosphate (DHAP)-dependent aldolases in the context of a multienzyme system

Sanchez-Moreno, Israel,Iturrate, Laura,Doyagueez, A Elisa G.,Martinez, Juan Antonio,Fernandez-Mayoralas, Alfonso,Garcia-Junceda, Eduardo

experimental part, p. 2967 - 2975 (2010/03/25)

The utility for carbon-carbon bond formation of a multienzyme system composed of recombinant dihydroxyacetone kinase (DHAK) from Citrobacter freundii, the fructose bisphosphate aldolase from rabbit muscle (RAMA) and acetate kinase (AK) for adenosine triphosphate (ATP) regeneration has been studied. Several aldehydes with great structural diversity, including three α,β-unsaturated aldehydes, have been analysed as acceptor substrates. It was found that α,β-unsaturated aldehydes bearing an electron-withdrawing group in the β position to the double bond with a trans configuration are good acceptors for RAMA in this multienzyme system. The aldol reaction proceeds with excellent D-threo enantioselectivity and the aldol adduct is obtained in good overall yield. The L-threo and D-erythro enantiomers are also accessible from rhamnulose 1-phosphate aldolase (Rha-1PA) and fuculose 1-phosphate aldolase (Fuc-1PA) catalysed reactions, respectively.

Fructose-1,6-diphosphate aldolase from spinach leaves, a challenger for enzymatic synthesis of ketoses

Valentin,Bolte

, p. 8103 - 8106 (2007/10/02)

Fructose-1,6-diphosphate aldolase is easily extracted from spinach leaves in a form sufficiently pure to be used in synthesis. Its specificity, different from that of the commercial rabbit muscle aldolase make it a new interesting tool for the synthesis of ketoses-1-phosphates.

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