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Phosphonic acid, P-[[3-hydroxy-4-(triphenylmethoxy)butoxy]methyl]-, bis(1-methylethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

918795-60-5

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918795-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918795-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,7,9 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 918795-60:
(8*9)+(7*1)+(6*8)+(5*7)+(4*9)+(3*5)+(2*6)+(1*0)=225
225 % 10 = 5
So 918795-60-5 is a valid CAS Registry Number.

918795-60-5SDS

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 [3-hydroxy-4-trityloxy-butoxymethyl]-phosphonic acid diisopropyl ester

1.2 Other means of identification

Product number -
Other names -

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:918795-60-5 SDS

918795-60-5Relevant academic research and scientific papers

An efficient synthesis of acyclic N7- and N9-adenine nucleosides via alkylation with secondary carbon electrophiles to introduce versatile functional groups at the C-1 position of acyclic moiety

Kotian, Pravin L.,Kumar, V. Satish,Lin, Tsu-Hsing,El-Kattan, Yahya,Ghosh, Ajit,Wu, Minwan,Cheng, Xiaogang,Bantia, Shanta,Babu, Yarlagadda S.,Chand, Pooran

, p. 121 - 140 (2007/10/03)

The introduction of versatile functional groups, allyl and ester, at the C-1 position of the acyclic chain in acyclic adenine nucleosides was achieved for the first time directly by alkylation of adenine and N6-protected adenine. Thus, the C-1′

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