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110333-20-5

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110333-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110333-20-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,3,3 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 110333-20:
(8*1)+(7*1)+(6*0)+(5*3)+(4*3)+(3*3)+(2*2)+(1*0)=55
55 % 10 = 5
So 110333-20-5 is a valid CAS Registry Number.

110333-20-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[5-oxo-4-(2-oxo-2-prop-2-enoxyethyl)-1,3-dioxolan-4-yl]acetic acid

1.2 Other means of identification

Product number -
Other names 2-<4-<(allyloxycarbonyl)methyl>-5-oxo-1,3-dioxolan-4-yl>acetic acid

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:110333-20-5 SDS

110333-20-5Downstream Products

110333-20-5Relevant articles and documents

The design and synthesis of nucleoside triphosphate isosteres as potential inhibitors of HIV reverse transcriptase

Weaver, Richard,Gilbert, Ian H.

, p. 5537 - 5562 (2007/10/03)

We describe the synthesis of a variety of lipophilic isosteres of nucleoside triphosphates as potential anti-HIV agents. The citrate molecule proved to be a good mimic of triphosphate by modelling in terms of charge and spatial distribution. Several lipophile derivatives of citrate were conjugated to the precedented anti-HIV nucleoside d4T via ester and amide linkages. A novel synthesis of 5'-amino-d4T is included. Intramolecular rearrangement of several amide-linked isosteres are also reported, along with an alternative synthetic strategy to the desired amide-linked isosteres.

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