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1376933-35-5

(R)-3-allyl-3-(phenylthio)indolin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1376933-35-5 Structure

  • Basic information

    1. Product Name: (R)-3-allyl-3-(phenylthio)indolin-2-one
    2. Synonyms: (R)-3-allyl-3-(phenylthio)indolin-2-one
    3. CAS NO:1376933-35-5
    4. Molecular Formula:
    5. Molecular Weight: 281.378
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1376933-35-5.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: (R)-3-allyl-3-(phenylthio)indolin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-3-allyl-3-(phenylthio)indolin-2-one(1376933-35-5)
    11. EPA Substance Registry System: (R)-3-allyl-3-(phenylthio)indolin-2-one(1376933-35-5)

  • 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: 1376933-35-5(Hazardous Substances Data)

1376933-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1376933-35-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,6,9,3 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1376933-35:
(9*1)+(8*3)+(7*7)+(6*6)+(5*9)+(4*3)+(3*3)+(2*3)+(1*5)=195
195 % 10 = 5
So 1376933-35-5 is a valid CAS Registry Number.

1376933-35-5Downstream Products

1376933-35-5Relevant articles and documents

Catalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles

Cai, Yunfei,Li, Jun,Chen, Weiliang,Xie, Mingsheng,Liu, Xiaohua,Lin, Lili,Feng, Xiaoming

, p. 2726 - 2729 (2012)

Catalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles has been developed via cooperative catalysis of a chiral N,N′-dioxide- Sc(OTf)3 complex and a Bronsted base. Utilizing readily available N-(phenylthio)phthalimide as the sulfur source, a wide range of optically active 3-phenylthiooxindoles were obtained in excellent yields with excellent enantioselectivities under mild reaction conditions.

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