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59997-14-7

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59997-14-7 Usage

General Description

10-ethyl-3-methylpyrimido[4,5-b]quinoline-2,4(3H,10H)-dione is a chemical compound with a complex and lengthy name. It belongs to the class of pyrimidoquinoline compounds and is characterized by its unique molecular structure. 10-ethyl-3-methylpyrimido[4,5-b]quinoline-2,4(3H,10H)-dione may have potential applications in medicinal chemistry, particularly in the development of novel drugs and pharmaceuticals. The specific properties and uses of this chemical compound are still under investigation, and further research is needed to fully understand its potential in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 59997-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,9 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59997-14:
(7*5)+(6*9)+(5*9)+(4*9)+(3*7)+(2*1)+(1*4)=197
197 % 10 = 7
So 59997-14-7 is a valid CAS Registry Number.

59997-14-7SDS

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 10-ethyl-3-methylpyrimido[4,5-b]quinoline-2,4-dione

1.2 Other means of identification

Product number -
Other names 10-ethyl-3-methyl-1,5-dihydro-5-deazaflavin

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:59997-14-7 SDS

59997-14-7Relevant articles and documents

A new synthetic approach to 5-deazaflavin and 5-deaza-10-thiaflavin

Chen,Tanaka,Yoneda

, p. 612 - 615 (2007/10/02)

A novel, one-step synthesis of 5-deazaflavin was developed, in which a [4 + 2]cycloaddition is presumably involved, to give the 5-deazaflavin derivative in moderate yield. This methodology was successfully applied to the stepwise preparation of its thio a

REACTIVITY OF 4a,5-EPOXY-5-DEAZAFLAVINS

Yoneda, Fumio,Sakuma, Yoshiharu

, p. 3977 - 3980 (2007/10/02)

Reactions of 4a,5-epoxy-5-deazaflavins with aqueous potassium carbonate, Vilsmeier reagent (dimethylformamide-phosphorus oxychloride), acetic anhydride-acetic acid, pyridine and triethanolamine gave the corresponding oxazolonoquinolines, 5-chloro-5-deazaflavins, 4a,5-diacetoxy-5-deazaflavins, l,5-dihydro-5-deazaflavin-5-ones, and deoxygenated 5-deazaflavins, respectively.

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