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CAS

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114469-27-1

2-benzyl-3-(tert-butylthio)propionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114469-27-1 Structure

  • Basic information

    1. Product Name: 2-benzyl-3-(tert-butylthio)propionic acid
    2. Synonyms: 2-benzyl-3-(tert-butylthio)propionic acid
    3. CAS NO:114469-27-1
    4. Molecular Formula:
    5. Molecular Weight: 252.378
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114469-27-1.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: 2-benzyl-3-(tert-butylthio)propionic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzyl-3-(tert-butylthio)propionic acid(114469-27-1)
    11. EPA Substance Registry System: 2-benzyl-3-(tert-butylthio)propionic acid(114469-27-1)

  • 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: 114469-27-1(Hazardous Substances Data)

114469-27-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114469-27-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,6 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 114469-27:
(8*1)+(7*1)+(6*4)+(5*4)+(4*6)+(3*9)+(2*2)+(1*7)=121
121 % 10 = 1
So 114469-27-1 is a valid CAS Registry Number.

114469-27-1Relevant articles and documents

Synthesis of tritium labelled thiorphan, an enkephalinase inhibitor

Wu, Shao-Yong,Masjedizadeh, Mohammad R.

body text, p. 23 - 28 (2009/05/09)

Tritium labelling of the enkephalinase inhibitor, thiorphan, is complicated by the presence of mercapto functional group. Reactions often used in aromatic tritiation, such as halogination and catalytic halogen/tritium displacement, are adversely affected

CYCLOPROPYL-ALANINE ARYL/ALKYLSULFIDE/SULFONYL-TERMINATED AMINO-DIOL COMPOUNDS FOR TREATMENT OF HYPERTENSION

-

, (2008/06/13)

Compounds characterized generally as cyclopropyl alanine aryl/alkylsulfide/sulfonyl-terminated amino diol derivatives are useful as renin inhibitors for the treatment of hypertension. Compounds of particular interest are those of the formula STR1 wherein

Synthesis and biological activity of some transition-state inhibitors of human renin

Buhlmayer,Caselli,Fuhrer,Goschke,Rasetti,Rueger,Stanton,Criscione,Wood

, p. 1839 - 1846 (2007/10/02)

A series of renin inhibitors containing the dipeptide transition state mimics (2S,4S,5S)-5-amino-4-hydroxy-2-isopropyl-7-methyloctanoic acid (Leu-(OH)-Val) and (2S,4S,5S)-5-amino-4-hydroxy-2-isopropyl-6-cyclohexylhexanoic acid (Cha-(OH)-Val) was prepared.

Antihypertensive 5-amino-4-hydroxyvaleryl derivatives substituted by sulphur-containing groups

-

, (2008/06/13)

Compounds of the formula STR1 in which R1 represents acyl substituted by a thio, sulphinyl or sulphonyl group, A represents an optionally N-alkylated α-amino acid residue that is bonded N-terminally to R1 and C-terminally to the grou

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