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1134206-50-0

BH3*AcSCH2P(C6H4-m-CH2CH2NMe2)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1134206-50-0 Structure

  • Basic information

    1. Product Name: BH3*AcSCH2P(C6H4-m-CH2CH2NMe2)2
    2. Synonyms: BH3*AcSCH2P(C6H4-m-CH2CH2NMe2)2
    3. CAS NO:1134206-50-0
    4. Molecular Formula:
    5. Molecular Weight: 458.072
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1134206-50-0.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: BH3*AcSCH2P(C6H4-m-CH2CH2NMe2)2(CAS DataBase Reference)
    10. NIST Chemistry Reference: BH3*AcSCH2P(C6H4-m-CH2CH2NMe2)2(1134206-50-0)
    11. EPA Substance Registry System: BH3*AcSCH2P(C6H4-m-CH2CH2NMe2)2(1134206-50-0)

  • 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: 1134206-50-0(Hazardous Substances Data)

1134206-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1134206-50-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,4,2,0 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1134206-50:
(9*1)+(8*1)+(7*3)+(6*4)+(5*2)+(4*0)+(3*6)+(2*5)+(1*0)=100
100 % 10 = 0
So 1134206-50-0 is a valid CAS Registry Number.

1134206-50-0Relevant articles and documents

Water-soluble phosphinothiol reagents

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Page/Page column 40; 46; 47, (2013/04/13)

Water soluble reagents and methods for the formation of an amide bond between a phosphinothioester and an azide in an aqueous medium. The phosphinothioester is generated using a water-soluble phosphinothiol reagent. This reaction allows formation of an amide bond between a wide variety of chemical species including amino acids, peptides or protein fragments in an aqueous solution. Of particular interest, this reaction allows for the formation of an amide bond in a physiological setting. In a specific embodiment, this invention provides reagents and methods for peptide ligation in an aqueous medium. The reaction eliminates the need for a cysteine residue and is traceless leaving no residual atoms in the ligated peptide product.

Coulombic effects on the traceless Staudinger ligation in water

Tam, Annie,Raines, Ronald T.

experimental part, p. 1055 - 1063 (2009/09/06)

The traceless Staudinger ligation can be mediated by phosphinothiols under physiological conditions. Proximal positive charges are necessary to achieve that transformation, presumably because those charges discourage protonation of the key iminophosphoran

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