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4-Pyridinamine,3-ethenyl-N,N-dimethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 191104-24-2 Structure
  • Basic information

    1. Product Name: 4-Pyridinamine,3-ethenyl-N,N-dimethyl-(9CI)
    2. Synonyms: 4-Pyridinamine,3-ethenyl-N,N-dimethyl-(9CI)
    3. CAS NO:191104-24-2
    4. Molecular Formula: C9H12N2
    5. Molecular Weight: 148.20498
    6. EINECS: N/A
    7. Product Categories: AMINETERTIARY;PYRIDINE
    8. Mol File: 191104-24-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-Pyridinamine,3-ethenyl-N,N-dimethyl-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Pyridinamine,3-ethenyl-N,N-dimethyl-(9CI)(191104-24-2)
    11. EPA Substance Registry System: 4-Pyridinamine,3-ethenyl-N,N-dimethyl-(9CI)(191104-24-2)
  • 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: 191104-24-2(Hazardous Substances Data)

191104-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 191104-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,1,0 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 191104-24:
(8*1)+(7*9)+(6*1)+(5*1)+(4*0)+(3*4)+(2*2)+(1*4)=102
102 % 10 = 2
So 191104-24-2 is a valid CAS Registry Number.

191104-24-2Upstream product

191104-24-2Downstream Products

191104-24-2Relevant articles and documents

Inhibitors of protein isoprenyl transferases

-

, (2008/06/13)

Compounds having the formula or a pharmaceutically acceptable salt thereof wherein R1 is (a) hydrogen, (b) loweralkyl, (c) alkenyl, (d) alkoxy, (e) thioalkoxy, (f) halo, (g) haloalkyl, (h) aryl-L2—, and (i) heterocyclic-L2—; R2 is selected from (a) (b) —C(O)NH—CH(R14)—C(O)OR15, (c) (d) —C(O)NH—CH(R14)—C(O)NHSO2R16 (e) —C(O)NH—CH(R14)-tetrazolyl, (f) —C(O)NH-heterocyclic, and (g) —C(O)NH—CH(R14)—C(O)NR17R18; R3 is heterocyclic, aryl, substituted or unsubstituted cycloalkyl; R4 is hydrogen, lower alkyl, haloalkyl, halogen, aryl, arylakyl, heterocyclic, or (heterocyclic)alkyl; L1 is absent or is selected from (a) —L4—N(R5)—L5—, (b) —L4—O—L5—, (c) —L4—S(O)n—L5— (d) —L4-L6—C(W)—N(R5)—L5—, (e) —L4-L6—S(O)m—N(R5)—L5—, (f) —L4—N(R5)—C(W)—L7-L5—, (g) —L4—N(R5)—S(O)p—L7—L5—, (h) optionally substituted alkylene, (i) optionally substituted alkenylene, and (j) optionally substituted alkynylene are inhibitors of protein isoprenyl transferases. Also disclosed are protein isoprenyl transferase inhibiting compositions and a method of inhibiting protein isoprenyl transferases.

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