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C12H14(2)HNO3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1255087-81-0 Structure
  • Basic information

    1. Product Name: C12H14(2)HNO3
    2. Synonyms:
    3. CAS NO:1255087-81-0
    4. Molecular Formula:
    5. Molecular Weight: 222.248
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1255087-81-0.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: C12H14(2)HNO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H14(2)HNO3(1255087-81-0)
    11. EPA Substance Registry System: C12H14(2)HNO3(1255087-81-0)
  • 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: 1255087-81-0(Hazardous Substances Data)

1255087-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1255087-81-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,5,0,8 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1255087-81:
(9*1)+(8*2)+(7*5)+(6*5)+(5*0)+(4*8)+(3*7)+(2*8)+(1*1)=160
160 % 10 = 0
So 1255087-81-0 is a valid CAS Registry Number.

1255087-81-0Downstream Products

1255087-81-0Relevant articles and documents

Enantioselective synthesis of α-deuterium labelled chiral α-amino acids via dynamic kinetic resolution of racemic azlactones

Oh, Joong-Suk,Kim, Kyung Il,Song, Choong Eui

supporting information; experimental part, p. 7983 - 7985 (2012/01/04)

Catalytic dynamic kinetic resolution (DKR) of racemic azlactones with EtOD using squaramide-based dimeric cinchona alkaloid organocatalysts is shown to be a highly effective strategy for the preparation of enantiomerically pure α-deuterated chiral α-amino

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