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1627210-82-5

C17H16N2O2S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1627210-82-5 Structure

  • Basic information

    1. Product Name: C17H16N2O2S
    2. Synonyms: C17H16N2O2S
    3. CAS NO:1627210-82-5
    4. Molecular Formula:
    5. Molecular Weight: 312.392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1627210-82-5.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: C17H16N2O2S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H16N2O2S(1627210-82-5)
    11. EPA Substance Registry System: C17H16N2O2S(1627210-82-5)

  • 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: 1627210-82-5(Hazardous Substances Data)

1627210-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1627210-82-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,7,2,1 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1627210-82:
(9*1)+(8*6)+(7*2)+(6*7)+(5*2)+(4*1)+(3*0)+(2*8)+(1*2)=145
145 % 10 = 5
So 1627210-82-5 is a valid CAS Registry Number.

1627210-82-5Downstream Products

1627210-82-5Relevant articles and documents

Palladium(II)-Catalyzed Reductive Cyclization of N-Tosyl-Tethered 1,7-Enynes: Enantioselective Synthesis of 1,2,3,4-Tetrahydroquinolines

Chen, Junjie,Han, Xiuling,Lu, Xiyan

, p. 8153 - 8157 (2019)

A novel Pd(II)-catalyzed reductive asymmetric cyclization of N-tosyl-tethered 1,7-enynes using ethanol as a hydrogen source is reported. This reaction provides facile ways for the synthesis of two types of 1,2,3,4-tetrahydroquinolines possessing a chiral

Intramolecular aminocyanation of alkenes by N-CN bond cleavage

Pan, Zhongda,Pound, Sarah M.,Rondla, Naveen R.,Douglas, Christopher J.

, p. 5170 - 5174 (2014/05/20)

A metal-free, Lewis acid promoted intramolecular aminocyanation of alkenes was developed. B(C6F5)3 activates N-sulfonyl cyanamides, thus leading to a formal cleavage of the N-CN bonds in conjunction with vicinal addition o

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