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61787-10-8

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61787-10-8 Usage

Chemical Properties

Off-White Solid

Uses

Different sources of media describe the Uses of 61787-10-8 differently. You can refer to the following data:
1. An intermediate for the preparation of 5?Deoxy-5-fluorouridine
2. An intermediate for the preparation of 5’-Deoxy-5-fluorouridine.

Check Digit Verification of cas no

The CAS Registry Mumber 61787-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,8 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61787-10:
(7*6)+(6*1)+(5*7)+(4*8)+(3*7)+(2*1)+(1*0)=138
138 % 10 = 8
So 61787-10-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H14FIN2O5/c1-12(2)20-7-6(3-14)19-10(8(7)21-12)16-4-5(13)9(17)15-11(16)18/h4,6-8,10H,3H2,1-2H3,(H,15,17,18)/t6-,7+,8?,10-/m1/s1

61787-10-8SDS

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 5-Chloro-5'-deoxy-5'-iodo-2',3'-O-isopropylidene-D-uridine

1.2 Other means of identification

Product number -
Other names 5'-Deoxy-5-fluoro-5'-iodo-2',3'-O-(1-methylethylidene)uridine

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:61787-10-8 SDS

61787-10-8Downstream Products

61787-10-8Relevant articles and documents

Process for the preparation of a deoxyuridine derivative

-

, (2008/06/13)

A process for the preparation of 5′-deoxy-5-fluorouridine, which comprises, the transformation of, 2′,3′-O-isopropylidene-5-fluorouridine in the corresponding 5′-O-sulfonyl derivative subsequent reaction with alkaline or earth-alkaline iodides and after hydrolysis of the isopropylidene group, reduction of the 5′-deoxy-5′-iodo-5 -fluorouridine thus obtained, is described.

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