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114021-22-6

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114021-22-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114021-22-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,0,2 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 114021-22:
(8*1)+(7*1)+(6*4)+(5*0)+(4*2)+(3*1)+(2*2)+(1*2)=56
56 % 10 = 6
So 114021-22-6 is a valid CAS Registry Number.

114021-22-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3',5'-BIS-O-(T-BUTYLDIMETHYLSILYL)-O4-(2,4,6-TRIISOPROPYL-PHENYLSULFONYL)THYMIDINE

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:114021-22-6 SDS

114021-22-6Relevant articles and documents

Quantification of the sixth DNA base hydroxymethylcytosine in the brain

Muenzel, Martin,Globisch, Daniel,Brueckl, Tobias,Wagner, Mirko,Welzmiller, Veronika,Michalakis, Stylianos,Mueller, Markus,Biel, Martin,Carell, Thomas

, p. 5375 - 5377 (2010)

Mind over matter: LC-MS has allowed the amount of the post-replicatively formed DNA base 5hydroxymethylcytosine (see picture; left) to be quantified in brain tissue. The nucleoside is most abundant in areas that are associated with higher cognitive functions, and its content in mouse hippocampi seems to increase with age. The new method enables hydroxymethylcytosine to be quantified with unprecedented accuracy. (Figure Presented)

Remarkable stabilization of antiparallel DNA triplexes by strong stacking effects of consecutively modified nucleobases containing thiocarbonyl groups

Yamada, Kenji,Hattori, Yusaku,Inde, Takeshi,Kanamori, Takashi,Ohkubo, Akihiro,Seio, Kohji,Sekine, Mitsuo

supporting information, p. 776 - 778 (2013/03/13)

The consecutive arrangement of 2′-deoxy-6-thioguanosines (s 6Gs) and 4-thiothymidines (s4Ts) in antiparallel triplex-forming oligonucleotides (TFOs) considerably stabilized the resulting antiparallel triplexes with high base recognit

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