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1H-Tetrazole-1-carboxylic acid, methyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59529-62-3

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59529-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59529-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,2 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59529-62:
(7*5)+(6*9)+(5*5)+(4*2)+(3*9)+(2*6)+(1*2)=163
163 % 10 = 3
So 59529-62-3 is a valid CAS Registry Number.

59529-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methoxycarbonyl tetrazolide

1.2 Other means of identification

Product number -
Other names 1-methoxycarbonyltetrazole

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:59529-62-3 SDS

59529-62-3Downstream Products

59529-62-3Relevant academic research and scientific papers

Tetrofuranose nucleoside phosphonic acids: Synthesis and properties

Polakova, Ivana,Budesinsky, Milos,Tocik, Zdenek,Rosenberg, Ivan

experimental part, p. 503 - 536 (2011/12/04)

New isoelectronic, non-isosteric phosphonate analogues of nucleoside 5'-phosphates featuring the phosphorus moiety directly attached on the sugar ring in the C4' position are described. The analogues were synthesised by a nucleosidation reaction from tetr

Alkylation, Acylation and Silylation of Azoles

Begtrup, Mikael,Larsen, Peter

, p. 1050 - 1057 (2007/10/02)

Performing alkylation, acylation and silylation reactions in separate deprotonation and nucleophilic displacement steps allows for better control of reaction conditions and facilitates problem handling in these processes.In the alkylation of azoles the alkylating agents and solvents possess individual reaction capabilities which seem to be approximately additive.Monoalkylation occurs if the sum of the normalized reaction potentials is equal or larger than the pKa value of the azole.Dialkylation is avoided by keeping the sum of the normalized reaction potentials below the pKa value of the alkylazole.The applicability of these principles is demonstrated by the development of effective procedures for the methylation, benzylation, acetylation, methoxycarbonylation and trimethylsilylation of azoles.

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