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14999-47-4

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14999-47-4 Usage

General Description

1-(2,3-anhydro-5-O-benzoylpentofuranosyl)pyrimidine-2,4(1H,3H)-dione is a chemical compound that is a derivative of pyrimidine-2,4(1H,3H)-dione. It is formed by the substitution of a benzoyl group at the 5-O position of the pentofuranosyl ring, and the removal of the 2,3-anhydro functionality in the sugar ring. 1-(2,3-anhydro-5-O-benzoylpentofuranosyl)pyrimidine-2,4(1H,3H)-dione is of interest in medicinal chemistry due to its potential pharmacological properties, and it may have applications as a drug or as a molecular probe in biological research. Its chemical structure and properties make it a valuable target for synthetic and analytical studies, and it may have potential uses in the development of novel pharmaceuticals or biologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 14999-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,9 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14999-47:
(7*1)+(6*4)+(5*9)+(4*9)+(3*9)+(2*4)+(1*7)=154
154 % 10 = 4
So 14999-47-4 is a valid CAS Registry Number.

14999-47-4SDS

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 Iso-E super

1.2 Other means of identification

Product number -
Other names Boisvelone

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:14999-47-4 SDS

14999-47-4Relevant articles and documents

An efficient route to pyrimidine nucleosides with the 2,3-anhydro-β-D-lyxofuranosyl stereochemistry

Callam, Christopher S.,Gadikota, Rajendrakumar Reddy,Lowary, Todd L.

, p. 1271 - 1274 (2007/10/03)

Described is the efficient preparation of 2,3-anhydro-β-D-lyxofuranosyl pyrimidine nucleosides via the coupling of a 2,3-anhydrosugar-containing glycosyl donor (5 or 6) with a silylated nucleoside base. The products are obtained with a high degree of stereoselectivity and in 65-77% yield.

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