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Carbamic acid, (1-methyl-4-pentenyl)-, phenylmethyl ester, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 113774-91-7 Structure
  • Basic information

    1. Product Name: Carbamic acid, (1-methyl-4-pentenyl)-, phenylmethyl ester, (R)-
    2. Synonyms:
    3. CAS NO:113774-91-7
    4. Molecular Formula: C14H19NO2
    5. Molecular Weight: 233.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113774-91-7.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: Carbamic acid, (1-methyl-4-pentenyl)-, phenylmethyl ester, (R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, (1-methyl-4-pentenyl)-, phenylmethyl ester, (R)-(113774-91-7)
    11. EPA Substance Registry System: Carbamic acid, (1-methyl-4-pentenyl)-, phenylmethyl ester, (R)-(113774-91-7)
  • 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: 113774-91-7(Hazardous Substances Data)

113774-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113774-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,7 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 113774-91:
(8*1)+(7*1)+(6*3)+(5*7)+(4*7)+(3*4)+(2*9)+(1*1)=127
127 % 10 = 7
So 113774-91-7 is a valid CAS Registry Number.

113774-91-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ((R)-1-Methyl-pent-4-enyl)-carbamic acid benzyl ester

1.2 Other means of identification

Product number -
Other names (R)-N-(benzyloxycarbonyl)-1-methyl-4-pentenylamine

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:113774-91-7 SDS

113774-91-7Relevant articles and documents

Protease inhibitors

-

, (2008/06/13)

The present invention provides C1-6alkyl-4-amino-azepan-3-one protease inhibitors and pharmaceutically acceptable salts, hydrates and solvates thereof which inhibit proteases, including cathepsin K, pharmaceutical compositions of such compounds, novel intermediates of such compounds, and methods for treating diseases of excessive bone loss or cartilage or matrix degradation, including osteoporosis; gingival disease including gingivitis and periodontitis; arthritis, more specifically, osteoarthritis and rheumatoid arthritis; Paget's disease; hypercalcemia of malignancy; and metabolic bone disease; and parasitic diseases, including malaria, by administering to a patient in need thereof one or more compounds of the present invention.

Protease inhibitors

-

Page/Page column 24, (2010/02/05)

The present invention provides C3-C6 1-amino-1-acyl cycloalkane-substituted 4-amino-azepan-3-one protease inhibitors and pharmaceutically acceptable salts, hydrates and solvates thereof which inhibit proteases, including cathepsin K,

Protease inhibitors

-

, (2008/06/13)

The present invention provides methods which use 4-amino-azepan-3-one protease inhibitors of cathepsin S in the treatment of diseases in which cathepsin S is implicated, especially treatment or prevention of autoimmune disease; treatment or prevention of a disease state caused by the formation of atherosclerotic lesions and complications arising therefrom; and diseases requiring inhibition, for therapy, of a class II MHC-restricted immune response, inhibition of an asthmatic response, inhibition of an allergic response, inhibition of immune response against a transplanted organ or tissue, or inhibition of elastase activity in atheroma, and novel compounds for use therewith.

THE SYNTHESIS OF EITHER (+) OR (-) TRANS-2,5-DIMETHYLPYRROLIDINE

Schlessinger, Richard H.,Iwanowicz, Edwin J.

, p. 2083 - 2086 (2007/10/02)

Trans-2,5-dimethylpyrrolidine, in either optical series, is prepared starting from D or L-alanine in an efficient and reasonably brief reaction sequence.

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