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77415-70-4

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77415-70-4 Usage

General Description

2,7-DIAZASPIRO[4.4]NONANE-1,3,6,8-TETRONE is a chemical compound with a spiro skeleton containing two nitrogen atoms. It is also known as diazaspiro nonanetetrone and has a unique molecular structure. 2,7-DIAZASPIRO[4.4]NONANE-1,3,6,8-TETRONE is a tetron isolated from biologically active marine bacterium that has demonstrated antibacterial properties, making it potentially useful in pharmaceutical applications. However, further research is needed to fully understand its properties and potential uses in medicine and other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 77415-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,1 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77415-70:
(7*7)+(6*7)+(5*4)+(4*1)+(3*5)+(2*7)+(1*0)=144
144 % 10 = 4
So 77415-70-4 is a valid CAS Registry Number.

77415-70-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-Diazaspiro[4.4]nonane-1,3,6,8-tetraone

1.2 Other means of identification

Product number -
Other names 2,7-Diazaspiro[4.4]nonane-1,3,6,8-tetrone

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:77415-70-4 SDS

77415-70-4Relevant articles and documents

First Kilogram-Scale Application of the Lanthanum Catalyzed Asymmetric Amination to Synthesis of the Chiral Succinimide Derivative, A Key Intermediate for the Preparation of AS-3201

Toshima, Minoru,Watanabe, Shoji,Uchiyama, Katsuya,Takasaki, Tsuyoshi,Bhogle, Nandkumar N.,Zhao, Hang,Filios, Mike,Takahashi, Kazuhiko,Snoonian, John R.,Saranteas, Kostas

, p. 1239 - 1245 (2016/07/23)

The process development of ethyl-(R)-3-amino-2,5-dioxopyrrolidine-3-carboxylate (2), the chiral intermediate for the manufacture of AS-3201 (1), is described. A practical and scalable Shibasaki asymmetric amination that generates the chiral quaternary center was developed and demonstrated on kilogram scale. A safe, convenient, and large-scale hydrogenation of the hydrazine intermediate was also developed.

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