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120966-81-6

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120966-81-6 Usage

General Description

The chemical (6R,9S)-3-methyl-7,8,9,10-tetrahydro-2H,6H-6,9-epoxypyrimido[2,1-b][1,3]oxazocin-2-one is a complex organic molecule with a Tetrahydro-2H,6H-6,9-epoxy structure. It contains a pyrimido-oxazocin ring system and a methyl group. This chemical is likely to have pharmaceutical or biological applications due to its complex structure and potential for interacting with biological systems. It could be used as a starting material in a synthesis or as a lead compound in drug discovery efforts. The unique structure of this chemical provides opportunities for further research and exploration in the field of medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 120966-81-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,9,6 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 120966-81:
(8*1)+(7*2)+(6*0)+(5*9)+(4*6)+(3*6)+(2*8)+(1*1)=126
126 % 10 = 6
So 120966-81-6 is a valid CAS Registry Number.

120966-81-6SDS

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 ddU-2,5'-anhydro-5-Me

1.2 Other means of identification

Product number -
Other names 2,5'-anhydro-3'-deoxythymidine

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:120966-81-6 SDS

120966-81-6Downstream Products

120966-81-6Relevant articles and documents

Stereoselective synthesis of 2',3'-dideoxy-nucleosides via intramolecular glycosylation of phenyl 1-seleno-glycosides. Synthesis of 2',3'-dideoxythymidine

Lluis, Jordi,Matheu, Ma. Isabel,Castillon, Sergio

, p. 1807 - 1810 (2007/10/03)

4-methoxy and 4-(2-trimethylsilylethoxy)pyrimidine bases were attached to the 5-position of the phenyl 2,3-dideoxy-1-seleno-glycero-pentofuranoside moiety. The presence of the silyl protecting group in the base is necessary to lead to neutral β-anhydro nucleosides by intramolecular glycosylation. The subsequent ring opening affords 3'-deoxythymidine with complete stereocontrol.

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