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Carbamic acid, [(methylamino)(methylthio)methylene]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

213739-25-4

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213739-25-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 213739-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,7,3 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 213739-25:
(8*2)+(7*1)+(6*3)+(5*7)+(4*3)+(3*9)+(2*2)+(1*5)=124
124 % 10 = 4
So 213739-25-4 is a valid CAS Registry Number.

213739-25-4SDS

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 tert-butyl(methylamino)(methylthio)methylenecarbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid, [(methylamino)(methylthio)methylene]-, 1,1-dimethylethyl ester

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:213739-25-4 SDS

213739-25-4Relevant academic research and scientific papers

Facile synthesis and fundamental properties of an: N -methylguanidine-bridged nucleic acid (GuNA[NMe])

Horie, Naohiro,Kumagai, Shinji,Kotobuki, Yutaro,Yamaguchi, Takao,Obika, Satoshi

supporting information, p. 6531 - 6536 (2018/10/02)

An N-methylguanidine-bridged nucleic acid (GuNA[NMe]), a guanidine-bridged nucleic acid (GuNA) bearing a methyl substituent at the bridge, was successfully synthesised and incorporated into oligonucleotides. By employing an acetyl protecting group, GuNA[NMe]-modified oligonucleotides bearing acid-sensitive purine nucleobases were successfully prepared. The obtained GuNA[NMe]-modified oligonucleotides exhibit excellent binding affinity towards the complementary single-stranded RNA and DNA. Furthermore, even a single GuNA[NMe] modification provides robust enzymatic stability, similar to that achieved by the well-established phosphorothioate backbone modification. These data indicate that such a GuNA[NMe] represents a valuable modification for the development of therapeutic oligonucleotides.

Novel aromatic compounds possessing antifungal or antibacterial activity

-

Page/Page column 53, (2010/02/06)

The present invention provides novel compounds possessing antibacterial, antifungal, antiviral, anticancer, and/or antiparasitic activities. Pharmaceutical compositions containing these compounds, methods of making and methods for using these compounds ar

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