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  • 1250870-01-9 Structure
  • Basic information

    1. Product Name: C18H18ClNO3
    2. Synonyms:
    3. CAS NO:1250870-01-9
    4. Molecular Formula:
    5. Molecular Weight: 331.799
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1250870-01-9.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: C18H18ClNO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H18ClNO3(1250870-01-9)
    11. EPA Substance Registry System: C18H18ClNO3(1250870-01-9)
  • 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: 1250870-01-9(Hazardous Substances Data)

1250870-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1250870-01-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,0,8,7 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1250870-01:
(9*1)+(8*2)+(7*5)+(6*0)+(5*8)+(4*7)+(3*0)+(2*0)+(1*1)=129
129 % 10 = 9
So 1250870-01-9 is a valid CAS Registry Number.

1250870-01-9Downstream Products

1250870-01-9Relevant articles and documents

Enantioselective Michael Addition of 2-Nitropropane to Substituted Chalcones and Chalcone Analogues Catalyzed by Chiral Crown Ethers Incorporating an α-D-Glucose or an α-D-Mannose Unit

Mako, Attila,Rapi, Zsolt,Drahos, Laszlo,Szoellosy, Aron,Keglevich, Gyoergy,Bako, Peter

, p. 424 - 431 (2010)

The chiral monoaza-15-crown-5 lariat ethers annellated to methyl-4,6-O-benzylidene-α-D-glucopyranoside-(1) or -mannopyranoside (2) used as phase transfer catalysts in the Michael addition of 2-nitropropane to substituted chalcones and chalcone analogues resulted in a significant asymmetric induction. The type of substituent on the chalcone molecule was found to have a significant influence on both the chemical yield and the enantioselectivity of the reaction: 24 novel chiral Michael adducts were prepared in 14-68% ee. These ee values were somewhat lower than that experienced in the case of the unsubstituted chalcone (85% ee). In the series of chalcone analogues*The 1-naphthyl Michael adduct was formed in 87% ee. Using glucose-based crown ether 1, Formation of the (+)-enantiomers was preferred, while applying mannose-based 2 as the catalyst, the (-)-enantiomers were in excess.

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