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153815-23-7

BOC-BETA,BETA-DIMETHYL-D-CYS(NPYS)-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 153815-23-7 Structure

  • Basic information

    1. Product Name: BOC-BETA,BETA-DIMETHYL-D-CYS(NPYS)-OH
    2. Synonyms: BOC-S-(3-NITRO-2-PYRIDINESULFENYL)-D-PENICILLAMINE;BOC-D-PEN(NPYS)-OH;BOC-D-PENICILLAMINE(NPYS)-OH;BOC-BETA,BETA-DIMETHYL-D-CYS(NPYS)-OH;Boc-b,b-diMethyl-D-Cys(NPys)-OH
    3. CAS NO:153815-23-7
    4. Molecular Formula: C15H21N3O6S2
    5. Molecular Weight: 403.47
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153815-23-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 558.5±50.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.37±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: -15°C
    8. Solubility: N/A
    9. PKA: 3.34±0.10(Predicted)
    10. CAS DataBase Reference: BOC-BETA,BETA-DIMETHYL-D-CYS(NPYS)-OH(CAS DataBase Reference)
    11. NIST Chemistry Reference: BOC-BETA,BETA-DIMETHYL-D-CYS(NPYS)-OH(153815-23-7)
    12. EPA Substance Registry System: BOC-BETA,BETA-DIMETHYL-D-CYS(NPYS)-OH(153815-23-7)

  • 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: 153815-23-7(Hazardous Substances Data)

153815-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153815-23-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,8,1 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 153815-23:
(8*1)+(7*5)+(6*3)+(5*8)+(4*1)+(3*5)+(2*2)+(1*3)=127
127 % 10 = 7
So 153815-23-7 is a valid CAS Registry Number.

153815-23-7Downstream Products

153815-23-7Relevant articles and documents

A new method for the preparation of 3-nitro-2-pyridinesulfenyl chloride and one-pot syntheses of N(α)-tert-butoxycarbonyl-S-3-nitro-2-pyridinesulfenyl derivatives of cysteine and D-penicillamine

Ueki,Honda,Kazama,Katoh

, p. 21 - 22 (2007/10/02)

3-Nitro-2-pyridinesulfenyl chloride was prepared by the reaction of benzyl 3-nitro-2-pyridyl sulfides with sulfuryl chloride. One-pot syntheses of N(α)-tert-butoxycarbonyl-S-3-nitro-2-pyridinesulfenyl derivatives of cysteine and D-penicillamine were accom

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