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261634-36-0

sulfamic acid 5-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-pentyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 261634-36-0 Structure

  • Basic information

    1. Product Name: sulfamic acid 5-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-pentyl ester
    2. Synonyms: sulfamic acid 5-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-pentyl ester
    3. CAS NO:261634-36-0
    4. Molecular Formula:
    5. Molecular Weight: 373.589
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 261634-36-0.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: sulfamic acid 5-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-pentyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: sulfamic acid 5-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-pentyl ester(261634-36-0)
    11. EPA Substance Registry System: sulfamic acid 5-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-pentyl ester(261634-36-0)

  • 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: 261634-36-0(Hazardous Substances Data)

261634-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 261634-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,6,3 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 261634-36:
(8*2)+(7*6)+(6*1)+(5*6)+(4*3)+(3*4)+(2*3)+(1*6)=130
130 % 10 = 0
So 261634-36-0 is a valid CAS Registry Number.

261634-36-0Upstream product

261634-36-0Downstream Products

261634-36-0Relevant articles and documents

The sulfamate functional group as a new anchor for solid-phase organic synthesis

Ciobanu, Liviu C.,Maltais, Rene,Poirier, Donald

, p. 445 - 448 (2000)

(Formula presented) Sulfamate derivatives were loaded on trityl chloride resin, and two variants of cleavage were developed for this sulfamate anchor: an acid treatment to easily restore the free sulfamate and a nucleophilic treatment to generate the corresponding phenol. In addition to loading/ cleavage assays and stability experiments, a model sequence of reactions was performed with the new sulfamate anchor to show its applicability in further combinatorial solid-phase synthesis of libraries of biologically relevant sulfamate derivatives.

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