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109280-15-1

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109280-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109280-15-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,2,8 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 109280-15:
(8*1)+(7*0)+(6*9)+(5*2)+(4*8)+(3*0)+(2*1)+(1*5)=111
111 % 10 = 1
So 109280-15-1 is a valid CAS Registry Number.

109280-15-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R)-(+)-camphor dimethyl acetal

1.2 Other means of identification

Product number -
Other names (+)-camphor dimethyl acetal

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:109280-15-1 SDS

109280-15-1Relevant articles and documents

5-[2-(2-Methoxy)bornyl]tetrazole as catalyst for dlastereoselective synthesis of 2′-deoxydlnucleoside (3′, 5′)-methylphosphonates

Schell, Peter,Engels, Joachim W.

, p. 769 - 772 (1997)

The synthesis of 5-[2-(2-methoxy)bornyl]tetrazole 1 is described. 1 is used as catalyst for the diastereoselective synthesis of some 2′-deoxy dinucleoside (3′, 5′)methylphosphonates in solution. Copyright 1997 by Marcel Dekker, Inc.

Synthesis of the core tetrasaccharide of Trypanosoma cruzi glycoinositolphospholipids: Manp(α1→6)-Manp(α1→4)-6-(2- aminoethylphosphonic acid)-GlcNp(α1→6)-myo-Ins-1-PO4

Hederos, Markus,Konradsson, Peter

, p. 7196 - 7207 (2007/10/03)

Synthesis of the core tetrasaccharide Manp(α1→6)- Manp(→1→4)-6-(2-aminoethylphosphonic acid)-GlcNp(α1→6)-myo- Ins-1-PO4, found in glycoinositolphospholipids of Trypanosoma cruzi parasites, is described. The key building block, 6-O-(2-azido-3-O-

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