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CAS

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849360-65-2

(3aR,8aS)-benzyl 3a-allyl-3,3a-dihydro-2H-furo[2,3-b]indole-8(8aH)-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 849360-65-2 Structure

  • Basic information

    1. Product Name: (3aR,8aS)-benzyl 3a-allyl-3,3a-dihydro-2H-furo[2,3-b]indole-8(8aH)-carboxylate
    2. Synonyms: (3aR,8aS)-benzyl 3a-allyl-3,3a-dihydro-2H-furo[2,3-b]indole-8(8aH)-carboxylate
    3. CAS NO:849360-65-2
    4. Molecular Formula:
    5. Molecular Weight: 335.403
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 849360-65-2.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: (3aR,8aS)-benzyl 3a-allyl-3,3a-dihydro-2H-furo[2,3-b]indole-8(8aH)-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3aR,8aS)-benzyl 3a-allyl-3,3a-dihydro-2H-furo[2,3-b]indole-8(8aH)-carboxylate(849360-65-2)
    11. EPA Substance Registry System: (3aR,8aS)-benzyl 3a-allyl-3,3a-dihydro-2H-furo[2,3-b]indole-8(8aH)-carboxylate(849360-65-2)

  • 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: 849360-65-2(Hazardous Substances Data)

849360-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849360-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,3,6 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 849360-65:
(8*8)+(7*4)+(6*9)+(5*3)+(4*6)+(3*0)+(2*6)+(1*5)=202
202 % 10 = 2
So 849360-65-2 is a valid CAS Registry Number.

849360-65-2Relevant articles and documents

Highly asymmetric bromocyclization of tryptophol: Unexpected accelerating effect of DABCO-derived bromine complex

Liu, Huan,Jiang, Guangde,Pan, Xixian,Wan, Xiaolong,Lai, Yisheng,Ma, Dawei,Xie, Weiqing

, p. 1908 - 1911 (2014/05/06)

Highly asymmetric bromocyclization of tryptophol by using chiral anionic phase-transfer catalyst and DABCO-derived brominating reagent is described. Optimization of the reaction conditions revealed that the reaction rate was accelerated together with impr

Total synthesis of (-)-physovenine from (-)-3a-hydroxyfuroindoline

Sunazuka, Toshiaki,Yoshida, Kiminari,Kojima, Naoto,Shirahata, Tatsuya,Hirose, Tomoyasu,Handa, Masaki,Yamamoto, Daisuke,Harigaya, Yoshihiro,Kuwajima, Isao,Omura, Satoshi

, p. 1459 - 1461 (2007/10/03)

Total synthesis of calabar bean alkaloid (-)-physovenine (-)-3 has been achieved in a concise manner starting from optically active (-)-3a- hydroxyfuroindoline (-)-2, synthesized via modified Sharpless epoxidation of tryptophol 1. Our strategy involved a

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