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29881-53-6

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29881-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29881-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,8 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29881-53:
(7*2)+(6*9)+(5*8)+(4*8)+(3*1)+(2*5)+(1*3)=156
156 % 10 = 6
So 29881-53-6 is a valid CAS Registry Number.

29881-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[5-(hydroxymethyl)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-6-yl]acetamide

1.2 Other means of identification

Product number -
Other names 3-(Acetylamino)-3-deoxy-1,2-O-(1-methylethylidene)pentofuranose

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:29881-53-6 SDS

29881-53-6Downstream Products

29881-53-6Relevant articles and documents

-

Brimacombe,Mofti

, p. 167,174 (1971)

-

Synthesis of tamiflu and its phosphonate congeners possessing potent anti-influenza activity

Shie, Jiun-Jie,Fang, Jim-Min,Wang, Shi-Yun,Tsai, Keng-Chang,Cheng, Yih-Shyun E.,Yang, An-Suei,Hsiao, Shih-Chia,Su, Ching-Yao,Wong, Chi-Huey

, p. 11892 - 11893 (2008/03/27)

Using d-xylose as an appropriate chiral precursor, we have synthesized active neuraminidase inhibitor oseltamivir, antiflu drug Tamiflu, and novel phosphonate congeners that exhibit even stronger antiflu activities by inhibiting the neuraminidases of the wild-type and H274Y mutant of H1N1 and H5N1 viruses. Molecular modeling of the neuraminidase-phosphonate complex indicates a pertinent binding mode of the phosphonate with three arginine residues in the active site. Discovery of such potent neuraminidase inhibitors will offer an opportunity to the development of new anti-influenza drugs. Copyright

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