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203312-38-3

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203312-38-3 Usage

Molecular structure

A complex organic compound with a spiro ring structure.

Hydroxy group

A polar, hydrophilic functional group (-OH) that can form hydrogen bonds.

Methoxy group

A functional group (-OCH3) that imparts some polarity and aromatic character.

4-Azaspiro ring

A nitrogen-containing spiro ring (azaspiro) that adds to the compound's complexity and potential pharmacological activity.

Dimethylphenyl group

Aromatic group with two methyl substituents (-CH3) that may contribute to the compound's aromatic properties.

Aromatic properties

The presence of the dimethylphenyl group suggests that the compound may exhibit aromatic characteristics.

Pharmacological or biological activity

The specific structure and functional groups of the compound indicate potential for pharmacological or biological activity, making it of interest for further study in medicinal chemistry or drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 203312-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,3,1 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 203312-38:
(8*2)+(7*0)+(6*3)+(5*3)+(4*1)+(3*2)+(2*3)+(1*8)=73
73 % 10 = 3
So 203312-38-3 is a valid CAS Registry Number.

203312-38-3SDS

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 3-(2,5-dimethylphenyl)-4-hydroxy-8-methoxy-1-azaspiro[4.5]dec-3-en-2-one

1.2 Other means of identification

Product number -
Other names Spirotetramat-enol

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:203312-38-3 SDS

203312-38-3Downstream Products

203312-38-3Relevant articles and documents

A High-Yield and Cost-Effective Synthesis of Spirotetramat

Mao, Longfei,Wang, Jiahao,Xu, Guiqing,Zhou, Yingjie

, p. 1775 - 1778 (2020)

Abstract: cis-8-Methoxy-1,3-diazaspiro[4.5]decane-2,4-dione, the key intermediate in the synthesis of spirotetramat, was synthesized by catalytic hydrogenation, oxidation, and Bucherer–Bergs reaction with 4-methoxycyclohexan-1-one as raw material. Spirotetramat was obtained in an overall yield of 20.4% by a multi-step reaction sequence including hydrolysis, esterification, acylation, intramolecular condensation, and O-acylation. The advantages of the proposed method are mild conditions, simple operation, and good to excellent yields in each step.

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