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CAS

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917887-43-5

Cyclohexanecarboxylic acid, 1-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxy-, methyl ester, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 917887-43-5 Structure

  • Basic information

    1. Product Name: Cyclohexanecarboxylic acid, 1-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxy-, methyl ester, cis-
    2. Synonyms:
    3. CAS NO:917887-43-5
    4. Molecular Formula: C13H23NO5
    5. Molecular Weight: 273.329
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 917887-43-5.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: Cyclohexanecarboxylic acid, 1-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxy-, methyl ester, cis-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanecarboxylic acid, 1-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxy-, methyl ester, cis-(917887-43-5)
    11. EPA Substance Registry System: Cyclohexanecarboxylic acid, 1-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxy-, methyl ester, cis-(917887-43-5)

  • 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: 917887-43-5(Hazardous Substances Data)

917887-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 917887-43-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,8,8 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 917887-43:
(8*9)+(7*1)+(6*7)+(5*8)+(4*8)+(3*7)+(2*4)+(1*3)=225
225 % 10 = 5
So 917887-43-5 is a valid CAS Registry Number.

917887-43-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name syn-1-[N-(t-butoxycarbonyl)amino]-4-hydroxycyclohexane-1-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl cis-1-tert.-butoxycarbonylamino-4-hydroxy-cyclohexanecarboxylate

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:917887-43-5 SDS

917887-43-5Relevant articles and documents

COMBINATIONS OF HEPATITIS C VIRUS INHIBITORS

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Page/Page column 604; 605, (2015/02/02)

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

Spirocyclic Heterocycles Medicaments Containing Said Compounds, Use Thereof And Method For Their Production

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Page/Page column 12, (2011/04/14)

The present invention relates to spirocyclic heterocycles of general formula (I) the tautomers, the stereoisomers, the mixtures thereof and the salts thereof, particularly the physiologically acceptable salts thereof with inorganic or organic acids, which

Stereoselective Synthesis of Amino Acid Analogs for Tumor Imaging

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Page/Page column 12, (2010/11/25)

The radiolabeled non-natural amino acid 1-amino-3-cyclobutane-1-carboxylic acid (ACBC) and its analogs are candidate tumor imaging agents useful for positron emission tomography and single photon emission computed tomography due to their selective affinity for tumor cells. The present invention provides methods for stereo-selective synthesis of syn-ACBC analogs. The disclosed synthetic strategy is reliable and efficient and can be used to synthesize a gram quantity of various syn-isomers of the ACBC analogs, particularly, syn-[18F]-1-amino-3-fluorocyclobutane-1-carboxylic acid (FACBC) and syn-[123I]-1-amino-3-iodocyclobutane-1-carboxylic (IACBC) acid analogs.

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