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tert-butyl 2-phenyl-1H-pyrrolo[3,2-b]pyridine-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1192159-95-7 Structure
  • Basic information

    1. Product Name: tert-butyl 2-phenyl-1H-pyrrolo[3,2-b]pyridine-1-carboxylate
    2. Synonyms: tert-butyl 2-phenyl-1H-pyrrolo[3,2-b]pyridine-1-carboxylate
    3. CAS NO:1192159-95-7
    4. Molecular Formula:
    5. Molecular Weight: 294.353
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1192159-95-7.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: tert-butyl 2-phenyl-1H-pyrrolo[3,2-b]pyridine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl 2-phenyl-1H-pyrrolo[3,2-b]pyridine-1-carboxylate(1192159-95-7)
    11. EPA Substance Registry System: tert-butyl 2-phenyl-1H-pyrrolo[3,2-b]pyridine-1-carboxylate(1192159-95-7)
  • 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: 1192159-95-7(Hazardous Substances Data)

1192159-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1192159-95-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,1,5 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1192159-95:
(9*1)+(8*1)+(7*9)+(6*2)+(5*1)+(4*5)+(3*9)+(2*9)+(1*5)=167
167 % 10 = 7
So 1192159-95-7 is a valid CAS Registry Number.

1192159-95-7Downstream Products

1192159-95-7Relevant articles and documents

Asymmetric Hydrogenation of Azaindoles: Chemo- and Enantioselective Reduction of Fused Aromatic Ring Systems Consisting of Two Heteroarenes

Makida, Yusuke,Saita, Masahiro,Kuramoto, Takahiro,Ishizuka, Kentaro,Kuwano, Ryoichi

supporting information, p. 11859 - 11862 (2016/11/16)

High enantioselectivity was achieved for the hydrogenation of azaindoles by using the chiral catalyst, which was prepared from [Ru(η3-methallyl)2(cod)] and a trans-chelating bis(phosphine) ligand (PhTRAP). The dearomative reaction exclusively occurred on the five-membered ring, thus giving the corresponding azaindolines with up to 97:3 enantiomer ratio.

Copper-catalyzed N-arylation/hydroamin(d)ation domino synthesis of indoles and its application to the preparation of a Chekl/KDR kinase inhibitor pharmacophore

Ackermann, Lutz,Barfuesser, Sebastian,Potukuchi, Harish K.

supporting information; experimental part, p. 1064 - 1072 (2010/03/03)

Inexpensive copper catalysts allow for efficient syntheses of N-aryl-, N-acyl-, or N-H-(aza)in-doles starting from ortho-alkynylbromoarenes. The broad scope of this domino N-arylation/hydro-amin(d)ation process is highlighted by the synthesis of highly fu

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