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Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-(1-pyrenylmethyl)-, 3'-(tetraethylphosphorodiamidite) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136838-01-2

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136838-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136838-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,3 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136838-01:
(8*1)+(7*3)+(6*6)+(5*8)+(4*3)+(3*8)+(2*0)+(1*1)=142
142 % 10 = 2
So 136838-01-2 is a valid CAS Registry Number.

136838-01-2SDS

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 5'-dimethoxytrityl-2'-(1-pyrenylmethyl)uridine 3'-phosphorobisdiethylamidite

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:136838-01-2 SDS

136838-01-2Downstream Products

136838-01-2Relevant academic research and scientific papers

Synthesis of oligonucleotide derivatives with pyrene group at sugar fragment

Yamana,Ohashi,Nunota,Kitamura,Nakano,Sangen,Shimidzu

, p. 6347 - 6350 (2007/10/02)

The synthesis of oligonucleotide derivatives possessing pyrene group at a specific sugar residue has been described. The incorporation of the pyrene was accomplished by preparation of the pyrene-modified uridine, 2'-(1-pyrenylmethyl)uridine, which was then converted to the protected phosphorobisdiethylamidite. This reagent was used for the solid-phase synthesis of oligonucleotide-pyrene conjugates. The purification of the conjugates was effected by reversed-phase HPLC. The oligonucleotide-pyrene conjugates synthesized here can bind to their complementary sequences with a cooperative interaction between the pyrene group and the adjacent base-pairs.

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