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3,4-Dihydro-4-oxo-spiro[2H-1-benzopyran-2,4'-piperidine]-1',6-dicarboxylic acid 1'-(1,1-dimethylethyl) ester is a complex ester derivative of spiro[2H-1-benzopyran-2,4'-piperidine]-1',6-dicarboxylic acid, featuring a tert-butyl group attached to the oxygen atom of the carboxylic acid functional group. This chemical compound holds potential pharmaceutical applications due to its structural resemblance to various bioactive compounds, such as benzopyran and piperidine derivatives, which may confer it with intriguing biological activities. However, further research is essential to elucidate its properties and potential uses comprehensively.

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  • 1'-(tert-butoxycarbonyl)-4-oxo-3H-spiro[1-benzopyran-2,4'-piperidine]-6-carboxylic acid

    Cas No: 921760-85-2

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  • 3,4-DIHYDRO-4-OXO-SPIRO[2H-1-BENZOPYRAN-2,4'-PIPERIDINE]-1',6-DICARBOXYLIC ACID 1'-(1,1-DIMETHYLETHYL) ESTER

    Cas No: 921760-85-2

  • USD $ 10.0-10.0 / Milligram

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  • 921760-85-2 Structure
  • Basic information

    1. Product Name: 3,4-DIHYDRO-4-OXO-SPIRO[2H-1-BENZOPYRAN-2,4'-PIPERIDINE]-1',6-DICARBOXYLIC ACID 1'-(1,1-DIMETHYLETHYL) ESTER
    2. Synonyms: 3,4-DIHYDRO-4-OXO-SPIRO[2H-1-BENZOPYRAN-2,4'-PIPERIDINE]-1',6-DICARBOXYLIC ACID 1'-(1,1-DIMETHYLETHYL) ESTER;tert-Butyl 6-carboxy-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylate
    3. CAS NO:921760-85-2
    4. Molecular Formula: C19H23NO6
    5. Molecular Weight: 361.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 921760-85-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,4-DIHYDRO-4-OXO-SPIRO[2H-1-BENZOPYRAN-2,4'-PIPERIDINE]-1',6-DICARBOXYLIC ACID 1'-(1,1-DIMETHYLETHYL) ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-DIHYDRO-4-OXO-SPIRO[2H-1-BENZOPYRAN-2,4'-PIPERIDINE]-1',6-DICARBOXYLIC ACID 1'-(1,1-DIMETHYLETHYL) ESTER(921760-85-2)
    11. EPA Substance Registry System: 3,4-DIHYDRO-4-OXO-SPIRO[2H-1-BENZOPYRAN-2,4'-PIPERIDINE]-1',6-DICARBOXYLIC ACID 1'-(1,1-DIMETHYLETHYL) ESTER(921760-85-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 921760-85-2(Hazardous Substances Data)

921760-85-2 Usage

Uses

Used in Pharmaceutical Industry:
3,4-Dihydro-4-oxo-spiro[2H-1-benzopyran-2,4'-piperidine]-1',6-dicarboxylic acid 1'-(1,1-dimethylethyl) ester is used as a precursor in the synthesis of pharmaceutical compounds for its structural similarity to bioactive benzopyran and piperidine derivatives. Its unique structure may contribute to the development of new drugs with potential therapeutic benefits.
Used in Research and Development:
In the field of medicinal chemistry, 3,4-Dihydro-4-oxo-spiro[2H-1-benzopyran-2,4'-piperidine]-1',6-dicarboxylic acid 1'-(1,1-dimethylethyl) ester serves as a valuable research compound for studying its biological activities and exploring its potential as a lead molecule in drug discovery. This can aid in the advancement of novel therapeutic agents and contribute to the understanding of its pharmacological profile.

Check Digit Verification of cas no

The CAS Registry Mumber 921760-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,1,7,6 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 921760-85:
(8*9)+(7*2)+(6*1)+(5*7)+(4*6)+(3*0)+(2*8)+(1*5)=172
172 % 10 = 2
So 921760-85-2 is a valid CAS Registry Number.

921760-85-2SDS

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 1'-[(2-methylpropan-2-yl)oxycarbonyl]-4-oxospiro[3H-chromene-2,4'-piperidine]-6-carboxylic acid

1.2 Other means of identification

Product number -
Other names A-1923

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:921760-85-2 SDS

921760-85-2Downstream Products

921760-85-2Relevant articles and documents

SPIROCHROMANON DERIVATIVES

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Page/Page column 113, (2008/12/07)

The invention relates to a compound of a general formula (I): wherein Ar1 represents a group formed from an aromatic ring selected from a group consisting of benzene, pyrazole, isoxazole, pyridine, indole, 1H-indazole, 1H-furo[2,3-c]pyrazole, 1H-thieno[2,3-c]pyrazole, benzimidazole, 1,2-benzisoxazole, imidazo[1,2-a]pyridine, imidazo[1,5-a]pyridine and 1H-pyrazolo[3,4-b]pyridine, having Ar2, and optionally having one or two or more substituents selected from R3; R1 and R2 each independently represent a hydrogen atom, a halogen atom, a cyano group, a C2-C6 alkenyl group, a C1-C6 alkoxy group, a C2-C7 alkanoyl group, a C2-C7 alkoxycarbonyl group, an aralkyloxycarbonyl group, a carbamoyl-C1-C6 alkoxy group, a carboxy-C2-C6 alkenyl group, or a group of -Q1-N(Ra)-Q2-Rb; or a C1-C6 alkyl group optionally having a substituent; or an aryl or heterocyclic group optionally having a substituent; or a C1-C6 alkyl group or a C2-C6 alkenyl group having the aryl or heterocyclic group; T and U each independently represent a nitrogen atom or a methine group; and V represents an oxygen atom or a sulfur atom. The compound of the invention is useful as therapeutical agents for various ACC-related diseases.

SPIROCHROMANONE DERIVATIVES AS ACETYL COENZYME A CARBOXYLASE (ACC) INHIBITORS

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Page/Page column 101-102, (2008/06/13)

The invention relates to a compound of a formula (I): , or a pharmaceutically acceptable salt or ester thereof, useful as a therapeutic agent for various ACC-related disorders.

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