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9-(5'-(2-oxo-1,3,2-dioxaphosphorinan-2-yl)-beta-arabinosyl)adenine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78000-58-5

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78000-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78000-58-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,0 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78000-58:
(7*7)+(6*8)+(5*0)+(4*0)+(3*0)+(2*5)+(1*8)=115
115 % 10 = 5
So 78000-58-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H18N5O7P/c14-11-8-12(16-5-15-11)18(6-17-8)13-10(20)9(19)7(25-13)4-24-26(21)22-2-1-3-23-26/h5-7,9-10,13,19-20H,1-4H2,(H2,14,15,16)/t7-,9-,10+,13?/m1/s1

78000-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-<5'-(2-oxo-1,3,2-dioxaphosphorinan-2-yl)-β-D-arabinofuranosyl>adenine

1.2 Other means of identification

Product number -
Other names 9-β-D-arabinofuranosyladenine-5'-<2-(2-oxo-1,3,2-dioxophosphorinane)>

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:78000-58-5 SDS

78000-58-5Downstream Products

78000-58-5Relevant academic research and scientific papers

Synthesis and Biological Evaluation of 9-adenine and 9-adenine: Potential Neutral Precursors of 9-adenine 5'-Monophosphate

Farquhar, David,Smith, Ronald

, p. 1358 - 1361 (2007/10/02)

9-adenine (1c) and 9-adenine (1d) were synthesized by reaction of 9-adenine with phosphoryl chloride with 1-amino-3-propanol and 1,3-propanediol, respectively. 1c consisted of a mixture of diastereoisomers, while 1d was enantiomerically homogeneous.The structures of these compounds were established by spectral (1H NMR, MS, UV) and elemental analyses.Both 1c and 1d were resistant to degradation by 5'-nucleotidase, alkaline phosphatase, venom phosphodisterase, crude snake venom, adenosine deaminase ,and adenylate deaminase.Neither compound was significantly biotransformed by mouse hepatic microsomal preparations in the presence of an NADPH-generating system.Compound 1c was marginally effective at prolonging the life span of mice bearing P-388 leukemia; compound 1d, however, was inactive.

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