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141214-26-8

1,4-Dioxa-7-azaspiro[4.4]nonane-8-carboxylic acid, 8-methyl-7-phenyl-6-thioxo-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141214-26-8 Structure

  • Basic information

    1. Product Name: 1,4-Dioxa-7-azaspiro[4.4]nonane-8-carboxylic acid, 8-methyl-7-phenyl-6-thioxo-, methyl ester
    2. Synonyms:
    3. CAS NO:141214-26-8
    4. Molecular Formula: C15H17NO4S
    5. Molecular Weight: 307.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141214-26-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,4-Dioxa-7-azaspiro[4.4]nonane-8-carboxylic acid, 8-methyl-7-phenyl-6-thioxo-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,4-Dioxa-7-azaspiro[4.4]nonane-8-carboxylic acid, 8-methyl-7-phenyl-6-thioxo-, methyl ester(141214-26-8)
    11. EPA Substance Registry System: 1,4-Dioxa-7-azaspiro[4.4]nonane-8-carboxylic acid, 8-methyl-7-phenyl-6-thioxo-, methyl ester(141214-26-8)

  • 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: 141214-26-8(Hazardous Substances Data)

141214-26-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141214-26-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,2,1 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141214-26:
(8*1)+(7*4)+(6*1)+(5*2)+(4*1)+(3*4)+(2*2)+(1*6)=78
78 % 10 = 8
So 141214-26-8 is a valid CAS Registry Number.

141214-26-8Relevant articles and documents

The influence of α-amido/thioamido functionality in ester reduction with sodium borohydride

Roy, Atanu,Bar, Narayan C.,Achari, Basudeb,Mandal, Sukhendu B.

, p. 644 - 650 (2007/10/03)

Sodium borohydride in methanol smoothly reduces the esters of α-amino acids having N-acyl (orthioacyl)-N-alkyl (-NRCOR′ or -NRCSR′) substituents, producing amino alcohol derivatives. Esters with α-NHCOR or-CONRR′ functionality however remain unaffected. Electron-withdrawing property of the substituent appears to play a crucial role, anion formation with -NHCOR group perhaps diminishing its effect.

A convenient reduction of substituted amino-acid esters

Mandal,Achari,Chattopadhyay

, p. 1647 - 1650 (2007/10/02)

Esters having N-alkyl-N-acyl (orthioacyl) functionality at the α-position are smoothly reduced with NaBH4-MeOH at 0-5°C in very good yields.

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