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adenosine 3',5'-monophosphodimethylamidate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40732-50-1

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40732-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40732-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,3 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40732-50:
(7*4)+(6*0)+(5*7)+(4*3)+(3*2)+(2*5)+(1*0)=91
91 % 10 = 1
So 40732-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H17N6O5P/c1-17(2)24(20,21)22-4-8-7(19)3-9(23-8)18-6-16-10-11(13)14-5-15-12(10)18/h3,5-6,8-9,19H,4H2,1-2H3,(H,20,21)(H2,13,14,15)/t8-,9-/m1/s1

40732-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name O3',O5'-dimethylaminophosphoryl-adenosine

1.2 Other means of identification

Product number -
Other names (4aR,6R,7R,7aS)-6-(6-Amino-purin-9-yl)-2-dimethylamino-2-oxo-tetrahydro-2λ5-furo[3,2-d][1,3,2]dioxaphosphinin-7-ol

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:40732-50-1 SDS

40732-50-1Downstream Products

40732-50-1Relevant academic research and scientific papers

ADENOSINE CYCLIC 3',5'-PHOSPHORAMIDATE AND N,N-DIMETHYLPHOSPHORAMIDATE: SYNTHESIS VIA SYMMETRICAL AND MIXED ANHYDRIDES AND HYDROLYSIS

Tomasz, Jenoe,Bottka, Sandor,Ludwig, Janos,Pelczer, Istvan

, p. 597 - 600 (2007/10/02)

The title compounds were synthesized by converting cyclic AMP with a sulfonyl chloride to the symmetrical anhydride or with diphenyl phosphorochloridate to the mixed anhydride, then aminolyzing the anhydrides without isolation.The synthesis preferentially gave SP-amides.Characteristic differences were observed in the behavior of the unsubstituted amide and the dimethylamide under hydrolysis conditions.

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