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1010686-71-1

C34H29N5O13 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1010686-71-1 Structure

  • Basic information

    1. Product Name: C34H29N5O13
    2. Synonyms:
    3. CAS NO:1010686-71-1
    4. Molecular Formula:
    5. Molecular Weight: 715.63
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1010686-71-1.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: C34H29N5O13(CAS DataBase Reference)
    10. NIST Chemistry Reference: C34H29N5O13(1010686-71-1)
    11. EPA Substance Registry System: C34H29N5O13(1010686-71-1)

  • 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: 1010686-71-1(Hazardous Substances Data)

1010686-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1010686-71-1 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, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1010686-71:
(9*1)+(8*0)+(7*1)+(6*0)+(5*6)+(4*8)+(3*6)+(2*7)+(1*1)=111
111 % 10 = 1
So 1010686-71-1 is a valid CAS Registry Number.

1010686-71-1Downstream Products

1010686-71-1Relevant 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.

, p. 1079 - 1082 (2008)

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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