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CAS

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261507-84-0

di-tert-butyl 5-hydroxydihydropyriMidine-1,3(2h,4h)-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 261507-84-0 Structure

  • Basic information

    1. Product Name: di-tert-butyl 5-hydroxydihydropyriMidine-1,3(2h,4h)-dicarboxylate
    2. Synonyms: di-tert-butyl 5-hydroxydihydropyriMidine-1,3(2h,4h)-dicarboxylate
    3. CAS NO:261507-84-0
    4. Molecular Formula: C14H26N2O5
    5. Molecular Weight: 302.36664
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 261507-84-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: di-tert-butyl 5-hydroxydihydropyriMidine-1,3(2h,4h)-dicarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: di-tert-butyl 5-hydroxydihydropyriMidine-1,3(2h,4h)-dicarboxylate(261507-84-0)
    11. EPA Substance Registry System: di-tert-butyl 5-hydroxydihydropyriMidine-1,3(2h,4h)-dicarboxylate(261507-84-0)

  • 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: 261507-84-0(Hazardous Substances Data)

261507-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 261507-84-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,5,0 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 261507-84:
(8*2)+(7*6)+(6*1)+(5*5)+(4*0)+(3*7)+(2*8)+(1*4)=130
130 % 10 = 0
So 261507-84-0 is a valid CAS Registry Number.

261507-84-0Downstream Products

261507-84-0Relevant articles and documents

COMPOUNDS, SALTS THEREOF AND METHODS FOR TREATMENT OF DISEASES

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Paragraph 00708; 00711; 00712, (2019/03/12)

The present disclosure relates to compounds according to Formulae disclosed herein, useful for treating diseases.

Synthesis and Characterization of 5-Substituted 1,3-Diazacyclohexane Derivatives

Axenrod, Theodore,Sun, Jianguang,Das, Kajal K.,Dave, Paritosh R.,Forohar, Farhad,Kaselj, Mira,Trivedi, Nirupam J.,Gilardi, Richard D.,Flippen-Anderson, Judith L.

, p. 1200 - 1206 (2007/10/03)

Three synthetic routes to 5-substituted 1,3-diazacyclohexane derivatives 1 are reported. The first method involves treatment of 1,3-diaminopropan-2-ol 2 with paraformaldehyde to yield 5-hydroxy-1,3-diazacyclohexane 3. A second method is based on the condensation of 2-bromo-2-nitro-1,3-propanediol with tert-butylamine and formaldehyde to yield 1,3-di-tert-butyl-5-bromo-5-nitro-1,3-diazacyclohexane 22. The third method relies on the cycloalkylation of methylenebisacetamide with 3-chloro-2-chloromethyl-2-propene to provide 5-exomethylene-1,3-diacetyl-1,3-diazacyclohexane 28. Functional group manipulations of 3, 22, and 28 provide a number of novel 1,3-diazacyclohexanes functionalized at the 5-position.

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