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122621-07-2

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122621-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122621-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,6,2 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 122621-07:
(8*1)+(7*2)+(6*2)+(5*6)+(4*2)+(3*1)+(2*0)+(1*7)=82
82 % 10 = 2
So 122621-07-2 is a valid CAS Registry Number.

122621-07-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2S,5R)-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl benzoate

1.2 Other means of identification

Product number -
Other names Thymidine,3'-deoxy-,5'-benzoate (9CI)

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:122621-07-2 SDS

122621-07-2Relevant articles and documents

Radical mediated synthesis of 3'-α-C-allenyl-2',3'-dideoxythymidine as a non-polar analogue of AZT

Becouarn,Czernecki,Valery

, p. 307 - 309 (1995)

The synthesis of the novel modified nucleoside (1) exhibiting the 1,2- propadienyl [allenyl] group at the 3'-α-position is described. The 3'-C-C bond was formed by radical reaction between triphenylprop 2-ynylstannane (2) and the 3'-bromo(iodo)-2',3'-dide

Synthesis of 2'-Deoxyribonucleosides: ?-3',5'-Di-O-benzoylthymidine [ Thymidine, 3',5'-dibenzoate ]

Prudhomme, Daniel R.,Park, Minnie,Wang, Zhiwei,Buck, Jason R.,Rizzo, Carmelo J.,Chambournier, Gilles,Djung, Jane,Hart, David J.

, p. 162 - 162 (2017/09/30)

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STEREOSELECTIVITIES IN THE COUPLING REACTION BETWEEN SILYLATED PYRIMIDINE BASES AND 1-HALO-2,3-DIDEOXYRIBOSE

Kawakami, Hiroshi,Ebata, Takashi,Koseki, Koshi,Matsumoto, Katsuya,Matsushita, Hajime,et al.

, p. 2041 - 2054 (2007/10/02)

Coupling reactions between 1-chloro-2,3-dideoxyribose and silylated pyrimidines have been examined from the point of stereoselectivity.When the reaction was carried out in chloroform, the selectivity was in the anomeric ratio of α:β = 4:6.On the other hand, the presence of tertiary amine raises the selectivity to α:β = 3:7.

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