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TERT-BUTYL N-(6-ISOTHIOCYANATOHEXYL)CARBAMATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

347890-44-2

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347890-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 347890-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,7,8,9 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 347890-44:
(8*3)+(7*4)+(6*7)+(5*8)+(4*9)+(3*0)+(2*4)+(1*4)=182
182 % 10 = 2
So 347890-44-2 is a valid CAS Registry Number.

347890-44-2SDS

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 tert-butyl N-(6-isothiocyanatohexyl)carbamate

1.2 Other means of identification

Product number -
Other names tert-butyl 6-isothiocyanatohexylcarbamate

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:347890-44-2 SDS

347890-44-2Relevant academic research and scientific papers

Versatile synthesis of 2′-amino-2′-deoxyuridine derivatives with a 2′-amino group carrying linkers possessing a reactive terminal functionality

Gondela, Andrzej,Tomczyk, Mateusz D.,Przypis, ?ukasz,Walczak, Krzysztof Z.

, p. 5626 - 5632 (2016)

2,2′-Anhydrouridine has been successfully converted into the appropriate 2′-amino-2′-deoxyuridine derivatives in a reaction with isothiocyanates obtained from amino acids or α,ω-diaminoalkanes. The initially formed oxazolidine-2-thione ring is cleaved under basic conditions into the corresponding 2′-amino(substituted)-2′-deoxyuridine derivatives. The implemented additional terminal functionality in the substituent attached to the 2′-amino group allows further modifications with e.g., fluorophore moiety.

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