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1010686-67-5

C27H25N3O9S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1010686-67-5 Structure

  • Basic information

    1. Product Name: C27H25N3O9S2
    2. Synonyms:
    3. CAS NO:1010686-67-5
    4. Molecular Formula:
    5. Molecular Weight: 599.642
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1010686-67-5.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: C27H25N3O9S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C27H25N3O9S2(1010686-67-5)
    11. EPA Substance Registry System: C27H25N3O9S2(1010686-67-5)

  • 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: 1010686-67-5(Hazardous Substances Data)

1010686-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1010686-67-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,0,6,8 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1010686-67:
(9*1)+(8*0)+(7*1)+(6*0)+(5*6)+(4*8)+(3*6)+(2*6)+(1*7)=115
115 % 10 = 5
So 1010686-67-5 is a valid CAS Registry Number.

1010686-67-5Downstream Products

1010686-67-5Relevant articles and documents

Stepwise cycloadditions of mesoionic systems: Thionation of thioisomunchnones by isothiocyanates

Cantillo, David,Avalos, Martin,Babiano, Reyes,Cintas, Pedro,Jimenez, Jose L.,Light, Mark E.,Palacios, Juan C.

supporting information; body text, p. 1079 - 1082 (2009/04/07)

An unusual thionation strategy of mesoionic compounds with aryl isothiocyanates enables a facile synthesis of 1,3-thiazolium-4-thiolate systems. The mechanistic pathway of such a transformation most likely involves a stepwise 1,3-dipolar cycioaddition, which is supported by theoretical calculations performed with a two-layer hybrid method (B3LYP/6-31G(d):PM3).

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