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1310538-74-9

1-allyl-N-tosyl-1H-indole-2-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1310538-74-9 Structure

  • Basic information

    1. Product Name: 1-allyl-N-tosyl-1H-indole-2-carboxamide
    2. Synonyms: 1-allyl-N-tosyl-1H-indole-2-carboxamide
    3. CAS NO:1310538-74-9
    4. Molecular Formula:
    5. Molecular Weight: 354.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1310538-74-9.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: 1-allyl-N-tosyl-1H-indole-2-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-allyl-N-tosyl-1H-indole-2-carboxamide(1310538-74-9)
    11. EPA Substance Registry System: 1-allyl-N-tosyl-1H-indole-2-carboxamide(1310538-74-9)

  • 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: 1310538-74-9(Hazardous Substances Data)

1310538-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1310538-74-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,5,3 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1310538-74:
(9*1)+(8*3)+(7*1)+(6*0)+(5*5)+(4*3)+(3*8)+(2*7)+(1*4)=119
119 % 10 = 9
So 1310538-74-9 is a valid CAS Registry Number.

1310538-74-9Relevant articles and documents

Carbamate-Catalyzed Enantioselective Bromolactamization

Cheng, Yi An,Yu, Wesley Zongrong,Yeung, Ying-Yeung

, p. 12102 - 12106 (2015)

A highly facile, efficient, and enantioselective bromolactamization of olefinic amides was effected by a carbamate catalyst and ethanol additive. The amide substrates underwent N-cyclization predominantly to give a diverse range of enantioenriched bromolactam products containing up to two stereogenic centers.

An unexpected Bromolactamization of Olefinic Amides Using a Three-Component Co-catalyst System

Cheng, Yi An,Yu, Wesley Zongrong,Yeung, Ying-Yeung

, p. 545 - 552 (2016/01/25)

Reaction between (N,N-dimethylamino)pyridine and isocyanate unexpectedly produced a three-component mixture. By using this mixture as an unprecedented three-component catalyst system, a facile and selective bromolactamization of olefinic amides has been developed. The protocol confers enhanced selectivity of N- over O-cyclization, leading to the formation of a structurally diverse range of lactams including both small and medium ring sizes.

A palladium-catalyzed aminoalkynylation strategy towards bicyclic heterocycles: Synthesis of (±)-trachelanthamidine

Nicolai, Stefano,Piemontesi, Cyril,Waser, Jerome

, p. 4680 - 4683 (2011/06/23)

Sweet cyclizations: The synthesis of pyrrolizidines and indolizidines has been achieved. Olefins were subjected to an intramolecular palladium-catalyzed aminoalkynylation with the hypervalent iodine reagent TIPS-EBX. After removal of the protecting group, a two-step cyclization sequence and subsequent reduction led to the natural product (±)-trachelanthamidine (see scheme; TIPS-EBX=triisopropylsilyl ethynylbenziodoxolone).

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