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1373883-04-5

C18H24N3O3(1+)*Cl(1-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1373883-04-5 Structure

  • Basic information

    1. Product Name: C18H24N3O3(1+)*Cl(1-)
    2. Synonyms: C18H24N3O3(1+)*Cl(1-)
    3. CAS NO:1373883-04-5
    4. Molecular Formula:
    5. Molecular Weight: 365.86
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1373883-04-5.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: C18H24N3O3(1+)*Cl(1-)(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H24N3O3(1+)*Cl(1-)(1373883-04-5)
    11. EPA Substance Registry System: C18H24N3O3(1+)*Cl(1-)(1373883-04-5)

  • 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: 1373883-04-5(Hazardous Substances Data)

1373883-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373883-04-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,8,8 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1373883-04:
(9*1)+(8*3)+(7*7)+(6*3)+(5*8)+(4*8)+(3*3)+(2*0)+(1*4)=185
185 % 10 = 5
So 1373883-04-5 is a valid CAS Registry Number.

1373883-04-5Downstream Products

1373883-04-5Relevant articles and documents

Ligand design for dual enantioselective control in Cu-catalyzed asymmetric conjugate addition of R2Zn to cyclic enone

Yoshimura, Misato,Shibata, Naoatsu,Kawakami, Miaki,Sakaguchi, Satoshi

experimental part, p. 3512 - 3518 (2012/06/04)

A new chiral N-heterocyclic carbene (NHC) ligand derived from a natural α-aminoester has been designed and synthesized. The coupling of N-methylbenzimidazole with an α-chloroacetamide derivative, which was prepared from chloroacetyl chloride and (S)-serin

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