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Carbamic acid, (4-hydroxy-1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI) is a complex chemical compound that combines elements such as carbon, hydrogen, nitrogen, and oxygen. It features a cyclohexyl group, which is a ring of six carbon atoms, and a hydroxy group, consisting of hydrogen and oxygen atoms. Carbamic acid, (4-hydroxy-1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI) is an ester, formed by the reaction of an alcohol and an acid, and is denoted by the "9CI" as it has been indexed in the 9th Collective Index of the Chemical Abstract Service (CAS). Carbamic acid, (4-hydroxy-1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI) is known for its utility in various chemical reactions and processes within the field of chemistry.

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  • 792913-83-8 Structure
  • Basic information

    1. Product Name: Carbamic acid, (4-hydroxy-1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI)
    2. Synonyms: Carbamic acid, (4-hydroxy-1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI);CarbaMic acid, (4-hydroxy-1-Methylcyclohexyl)-, 1,1-diMethylethyl ester;2-Methyl-2-propanyl(4-hydroxy-1-Methylcyclohexyl)carbaMate;tert-Butyl (4-hydroxy-1-Methylcyclohexyl)carbaMate;(4-Hydroxy-1-methyl-cyclohexyl)-carbamic acid tert-butyl ester;tert-butyl N-(4-hydroxy-1-methylcyclohexyl)carbamate;(4-hydroxy-1-methylcyclohexyl)Carbamic acid 1,1-dimethylethyl ester
    3. CAS NO:792913-83-8
    4. Molecular Formula: C12H23NO3
    5. Molecular Weight: 229.31592
    6. EINECS: N/A
    7. Product Categories: METHYL
    8. Mol File: 792913-83-8.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.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: Carbamic acid, (4-hydroxy-1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, (4-hydroxy-1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI)(792913-83-8)
    11. EPA Substance Registry System: Carbamic acid, (4-hydroxy-1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI)(792913-83-8)
  • 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: 792913-83-8(Hazardous Substances Data)

792913-83-8 Usage

Uses

Used in Chemical Reactions:
Carbamic acid, (4-hydroxy-1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI) is used as a reactant in various chemical reactions for its unique structural properties and reactivity.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Carbamic acid, (4-hydroxy-1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI) is used as an intermediate in the synthesis of certain drugs, leveraging its chemical reactivity and structural characteristics to facilitate the production of medicinal compounds.
Used in Research and Development:
Carbamic acid, (4-hydroxy-1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI) is employed as a research compound in academic and industrial laboratories, where its properties are studied to understand its potential applications and to develop new methodologies in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 792913-83-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,2,9,1 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 792913-83:
(8*7)+(7*9)+(6*2)+(5*9)+(4*1)+(3*3)+(2*8)+(1*3)=208
208 % 10 = 8
So 792913-83-8 is a valid CAS Registry Number.

792913-83-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(4-hydroxy-1-methylcyclohexyl)carbamate

1.2 Other means of identification

Product number -
Other names tert-Butyl (4-hydroxy-1-methylcyclohexyl)carbamate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:792913-83-8 SDS

792913-83-8Relevant articles and documents

INHIBITORS OF RAF KINASES

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Paragraph 00461-00463, (2021/04/30)

Provided herein are inhibitors of receptor tyrosine kinase effector, RAF, pharmaceutical compositions comprising said compounds, and methods for using said compounds for the treatment of diseases.

Novel Compounds for the Treatment of Diseases Associated with Amyloid or Amyloid-Like Proteins

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, (2011/11/30)

The present invention relates to novel compounds that can be employed in the treatment of a group of disorders and abnormalities associated with amyloid protein, such as Alzheimer's disease, and of diseases or conditions associated with amyloid-like proteins. The compounds of the present invention can also be used in the treatment of ocular diseases associated with pathological abnormalities/changes in the tissues of the visual system. The present invention further relates to pharmaceutical compositions comprising these compounds and to the use of these compounds for the preparation of medicaments for treating or preventing diseases or conditions associated with amyloid and/or amyloid-like proteins. A method of treating or preventing diseases or conditions associated with amyloid and/or amyloid-like proteins is also disclosed.

2-CYANOPYRROLIDINE DERIVATIVES AND THEIR USE AS DPP-IV INHIBITORS

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Page 30, (2010/02/09)

A compound of the formula (I) or a pharmaceutically acceptable salt thereof: [wherein X is CFH, or CF?2#191, R?1? is the moiety represented by the formula: [wherein R?2? is (lower) alkyl, R?3? is phenyl-(lower)alkyl, and the like.], and the like.] Compounds of formula (I) inhibit DPP-IV activity. They are therefore useful in the treatment of conditions mediated by DPP-IV, such as NIDDM.

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