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thymine-acetic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

272788-85-9

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272788-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 272788-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,2,7,8 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 272788-85:
(8*2)+(7*7)+(6*2)+(5*7)+(4*8)+(3*8)+(2*8)+(1*5)=189
189 % 10 = 9
So 272788-85-9 is a valid CAS Registry Number.

272788-85-9SDS

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 N1-tert-butyloxycarbonylmethylthymine

1.2 Other means of identification

Product number -
Other names tert-butyl (thymin-1-yl)acetate

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:272788-85-9 SDS

272788-85-9Relevant academic research and scientific papers

New thymine-based derivative of nitrogen mustards

Boens, Benjamin,Teste, Karine,Hadj-Bouazza, Amel,Ismaili, Jihane,Zerrouki, Rachida

, p. 197 - 205 (2012)

This work deals with the synthesis of a new nitrogen mustard derivative based on thymine. To introduce the bis(2-chloroethyl)amine group to position 4 of the pyrimidine base, many strategies were explored and the desired compound was finally obtained, thanks to a synthetic pathway in five steps. Copyright Taylor and Francis Group, LLC.

Design of a new oligotriazole peptide nucleic acid analogue (oT-PNA)

Vergnaud, Julien,Faugeras, Pierre-Antoine,Chaleix, Vincent,Champavier, Yves,Zerrouki, Rachida

, p. 6185 - 6189 (2011)

We describe in this Letter the synthesis of an original thymine azido-heterotrimer generated by Click Chemistry. This trimer has been obtained from an azido-thymidine and a new chloroethyl-propargylated PNA monomer analogue, after two azidation/click-reaction cycles. Conformational preferences of a rotameric intermediate have also been studied.

Synthesis and hybridization properties of DNA-PNA chimeras carrying 5- bromouracil and 5-methylcytosine

Ferrer, Elisenda,Shevchenko, Anna,Eritja, Ramon

, p. 291 - 297 (2007/10/03)

The preparation of 5-bromouracil and 5-methylcytosine peptide nucleic acid (PNA) monomers is described. These PNA monomers were used for the preparation of several DNA-PNA chimeras and their hybridization properties are described. The substitution of cyto

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