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2863-04-9

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2863-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2863-04-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,6 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2863-04:
(6*2)+(5*8)+(4*6)+(3*3)+(2*0)+(1*4)=89
89 % 10 = 9
So 2863-04-9 is a valid CAS Registry Number.

2863-04-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Thymidine 3',5'-diphosphate

1.2 Other means of identification

Product number -
Other names THYMIDINE-3',5'-DIPHOSPHATE

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:2863-04-9 SDS

2863-04-9Downstream Products

2863-04-9Relevant articles and documents

-

Tsumita,Chargaff

, p. 568,573,574 (1958)

-

A 13Cmr study of 2'-deoxynucleotides in the syn and anti conformation

Niemczura, Walter P.,Hruska, Frank E.

, p. 472 - 478 (2007/10/02)

The geminal and vicinal 13C-31P coupling constants for the 3'- and 5'-monophosphates and 3',5'-diphosphates of thymidine and its isomer 6-methyl-2'-deoxyuridine have been obtained for aqueous solutions at various pH values.Since the thymine base is anti and the 6-methyluracil base is syn, the data provide information about the influence of the orientation about the N-glycosyl linkage on the conformation about the C(5')-O(5')(φ) and C(3')-O(3')(φ') bonds.The 3J(C4'-P5') couplings reveal a preference for the t(φ) conformer of the 5'-nucleotidyl units, in agreement with previous measurements of 1H-31P coupling constants.The 3J(C4'- P3') and 3J(C2'-P3') couplings are consistent with a preference for the t(φ') conformer for both the syn and anti 3'-nucleotidyl units.The response of these couplings to secondary ionization of the phosphate is different for the thymine and 5-methyluracil derivatives and suggests a phosphate-phosphate interaction for the syn, but not the anti, 3',5'-diphosphates.A correlation between the sugar-pucker and the φ' orientation is revealed.The 2J(C5'-P5') and 2J(C3'-P3') are relatively insensitive to the ionization state of the phosphate as well as to other structural features of the deoxyribose phosphate backbone.

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