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158665-27-1

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158665-27-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158665-27-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,6,6 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 158665-27:
(8*1)+(7*5)+(6*8)+(5*6)+(4*6)+(3*5)+(2*2)+(1*7)=171
171 % 10 = 1
So 158665-27-1 is a valid CAS Registry Number.

158665-27-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name SPACER-C 12 CEP

1.2 Other means of identification

Product number -
Other names -

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:158665-27-1 SDS

158665-27-1Downstream Products

158665-27-1Relevant articles and documents

Modular Strategy to Expand the Chemical Diversity of DNA and Sequence-Controlled Polymers

De Rochambeau, Donatien,Sun, Yuanye,Barlog, Maciej,Bazzi, Hassan S.,Sleiman, Hanadi F.

, p. 9774 - 9786 (2018)

Sequence-defined polymers with customizable sequences, monodispersity, substantial length, and large chemical diversity are of great interest to mimic the efficiency and selectivity of biopolymers. We report an efficient, facile, and scalable synthetic route to introduce many chemical functionalities, such as amino acids and sugars in nucleic acids and sequence-controlled oligophosphodiesters. Through achiral tertiary amine molecules that are perfectly compatible with automated DNA synthesis, readily available amines or azides can be turned into phosphoramidites in two steps only. Individual attachment yields on nucleic acids and artificial oligophosphodiesters using automated solid-phase synthesis (SPS) were >90% in almost all cases. Using this method, multiple water-soluble sequence-defined oligomers bearing a range of functional groups in precise sequences could be synthesized and purified in high yields. The method described herein significantly expands the library of available functionalities for nucleic acids and sequence-controlled polymers.

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