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83707-14-6

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  • Adenosine, cyclic3',5'-(hydrogen phosphate), 2'-[2-(methylamino)benzoate]

    Cas No: 83707-14-6

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83707-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83707-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,0 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83707-14:
(7*8)+(6*3)+(5*7)+(4*0)+(3*7)+(2*1)+(1*4)=136
136 % 10 = 6
So 83707-14-6 is a valid CAS Registry Number.

83707-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name MANT-CAMP SODIUM SALT

1.2 Other means of identification

Product number -
Other names ADENOSINE 3',5'-CYCLIC MONOPHOSPHATE,2'-O-(N-METHYLANTHRANILOYL)-,SODIUM SALT

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:83707-14-6 SDS

83707-14-6Downstream Products

83707-14-6Relevant articles and documents

RNA structure analysis at single nucleotide resolution by Selective 2′-Hydroxyl Acylation and Primer Extension (SHAPE)

Merino, Edward J.,Wilkinson, Kevin A.,Coughlan, Jennifer L.,Weeks, Kevin M.

, p. 4223 - 4231 (2005)

The reactivity of an RNA ribose hydroxyl is shown to be exquisitely sensitive to local nucleotide flexibility because a conformationally constrained adjacent 3′-phosphodiester inhibits formation of the deprotonated, nucleophilic oxyanion form of the 2′-hydroxyl group. Reaction with an appropriate electrophile, N-methylisatoic anhydride, to form a 2′-O-adduct thus can be used to monitor local structure at every nucleotide in an RNA. We develop a quantitative approach involving Selective 2′-Hydroxyl Acylation analyzed by Primer Extension (SHAPE) to map the structure of and to distinguish fine differences in structure for tRNAAsp transcripts at single nucleotide resolution. Modest extensions of the SHAPE approach will allow RNA structure to be monitored comprehensively and at single nucleotide resolution for RNAs of arbitrary sequence and structural complexity and under diverse solution environments.

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