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13387-98-9

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13387-98-9 Usage

Compound type

Complex chemical compound

Derivative of

Pentitol (a sugar alcohol)

Acetylation

Tri-acetate derivative (acetylated at three positions)

Bicyclic heterocycle

Pyrazolo[4,3-d]pyrimidin-3-yl group

Potential applications

Pharmaceutical and medicinal chemistry

Biological activity

May exhibit biological activity

Synthesis building block

Can be used for synthesizing other complex molecules

Further research

Properties and uses need to be determined through additional research and testing

Check Digit Verification of cas no

The CAS Registry Mumber 13387-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,8 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13387-98:
(7*1)+(6*3)+(5*3)+(4*8)+(3*7)+(2*9)+(1*8)=119
119 % 10 = 9
So 13387-98-9 is a valid CAS Registry Number.

13387-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Triacetylformycin B

1.2 Other means of identification

Product number -
Other names ELPETRIGINE

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:13387-98-9 SDS

13387-98-9Relevant articles and documents

The design and synthesis of inhibitors of adenosine 5'-monophosphate deaminase

Lindell, Stephen D.,Moloney, Brian A.,Hewitt, Brian D.,Earnshaw, Christopher G.,Dudfield, Philip J.,Dancer, Jane E.

, p. 1985 - 1990 (1999)

Carbocylic coformycin (4) is a potent herbicide whose primary mode of action involves inhibition of adenosine 5'-monophosphate deaminase (AMPDA) following phosphorylation of the 5'-hydroxyl group in vivo. The search for more stable and accessible structures led to the synthesis of carbocyclic nebularine (8) and deaminoformycin (10). The latter compound is a good herbicide and its corresponding 5'-monophosphate 14 is a strong inhibitor of plant AMPDA (IC50 100 nM).

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