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1423165-67-6

C18H31NO3SSi is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1423165-67-6 Structure

  • Basic information

    1. Product Name: C18H31NO3SSi
    2. Synonyms: C18H31NO3SSi
    3. CAS NO:1423165-67-6
    4. Molecular Formula:
    5. Molecular Weight: 369.601
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1423165-67-6.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: C18H31NO3SSi(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H31NO3SSi(1423165-67-6)
    11. EPA Substance Registry System: C18H31NO3SSi(1423165-67-6)

  • 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: 1423165-67-6(Hazardous Substances Data)

1423165-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1423165-67-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,3,1,6 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1423165-67:
(9*1)+(8*4)+(7*2)+(6*3)+(5*1)+(4*6)+(3*5)+(2*6)+(1*7)=136
136 % 10 = 6
So 1423165-67-6 is a valid CAS Registry Number.

1423165-67-6Relevant articles and documents

Syntheses of five- and seven-membered ring sultam derivatives by Michael addition and Baylis-Hillman reactions

Tong, Kun,Tu, Jinchang,Qi, Xueyong,Wang, Min,Wang, Yanjie,Fu, Haizhen,Pittman Jr., Charles U.,Zhou, Aihua

supporting information, p. 2369 - 2375 (2013/03/29)

Five- and seven-membered sultam derivatives were conveniently synthesized via intra- or intermolecular Michael additions and an improved vinyl sulfonamide Baylis-Hillman reaction. Two different cyclization pathways were explored for the oxa-Michael reaction. A good solvent was discovered for an otherwise sluggish ketone-type Baylis-Hillman reaction in which vinyl sulfonamide ketones were used as the precursors. Furthermore, a strong base caused vinyl sulfonamide ketones to undergo 5-endo-trig intramolecular cyclizations, which are disfavored according to Baldwin's rule. Finally Baylis-Hillman reaction products were used as scaffolds for diversity-oriented sultam syntheses.

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