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7-Chlorobenzo[g]pteridine-2,4(1H,3H)-dione is a chemical compound with the molecular formula C7H4ClN5O2. It is a derivative of pteridine, a heterocyclic organic compound with a pyrimido[4,5-b]pyrazine core structure. The presence of a chlorine atom at the 7-position and two carbonyl groups at the 2 and 4 positions distinguishes 7-chlorobenzo[g]pteridine-2,4(1H,3H)-dione from other pteridines. This specific chemical structure may confer unique properties and potential applications in various fields, such as pharmaceuticals or chemical research. However, without additional context or specific information on its synthesis, reactivity, or uses, a more detailed summary cannot be provided.

3273-42-5

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3273-42-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3273-42-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,7 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3273-42:
(6*3)+(5*2)+(4*7)+(3*3)+(2*4)+(1*2)=75
75 % 10 = 5
So 3273-42-5 is a valid CAS Registry Number.

3273-42-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chloro-1H-benzo[g]pteridine-2,4-dione

1.2 Other means of identification

Product number -
Other names 7-Chloroalloxazine

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:3273-42-5 SDS

3273-42-5Downstream Products

3273-42-5Relevant academic research and scientific papers

INVESTIGATION IN THE ALLOXAZINE AND ISOALLOXAZINE SERIES. LV. SYNTHESIS AND PROPERTIES OF 7-AMINO-SUBSTITUTED ALLOXAZINES

Tul'chinskaya, L. S.,Polyakova, N. A.,Zapesochnaya, L. G.,Karlstedt, N. B.,Gyach, N. V.,et al.

, p. 917 - 923 (2007/10/02)

7-Aminoalloxazine and its derivatives (7-acetylaminoalloxazine and 1,3-dimethyl-7-aminoalloxazine) were synthesized.The introduction of an amino group at position 7 of the alloxazine molecule leads to a substantial decrease in the energy of the long-wave

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