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benzyl 8-oxa-4-azabicyclo[5.1.0]octane-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 501121-89-7 Structure
  • Basic information

    1. Product Name: benzyl 8-oxa-4-azabicyclo[5.1.0]octane-4-carboxylate
    2. Synonyms: benzyl 8-oxa-4-azabicyclo[5.1.0]octane-4-carboxylate
    3. CAS NO:501121-89-7
    4. Molecular Formula: C14H17NO3
    5. Molecular Weight: 247.28968
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 501121-89-7.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: benzyl 8-oxa-4-azabicyclo[5.1.0]octane-4-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl 8-oxa-4-azabicyclo[5.1.0]octane-4-carboxylate(501121-89-7)
    11. EPA Substance Registry System: benzyl 8-oxa-4-azabicyclo[5.1.0]octane-4-carboxylate(501121-89-7)
  • 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: 501121-89-7(Hazardous Substances Data)

501121-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501121-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,1,2 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 501121-89:
(8*5)+(7*0)+(6*1)+(5*1)+(4*2)+(3*1)+(2*8)+(1*9)=87
87 % 10 = 7
So 501121-89-7 is a valid CAS Registry Number.

501121-89-7SDS

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 benzyl 8-oxa-4-azabicyclo[5.1.0]octane-4-carboxylate

1.2 Other means of identification

Product number -
Other names 8-Oxa-4-aza-bicyclo[5.1.0]octane-4-carboxylic acid benzyl ester

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:501121-89-7 SDS

501121-89-7Relevant articles and documents

AZEPANE DERIVATIVES AND METHODS OF TREATING HEPATITIS B INFECTIONS

-

, (2015/07/22)

Provided herein are compounds useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.

AZEPANE DERIVATIVES AND METHODS OF TREATING HEPATITIS B INFECTIONS

-

, (2015/09/22)

Provided herein are compounds useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.

NOVEL COMPOUNDS

-

, (2013/06/26)

This invention relates to compounds of formula I their use as positive allosteric modulators of mGlu5 receptor activity, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of neurological and psychiatric disorders associated with glutamate dysfunction such as schizophrenia or cognitive decline such as dementia or cognitive impairment. A, B, X, R1, R2, R3 have meanings given in the description.

NOVEL COMPOUNDS

-

, (2013/06/27)

This invention relates to compounds of formula I their use as positive allosteric modulators of mGlu5 receptor activity, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of neurological and psychiatric disorders associated with glutamate dysfunction such as schizophrenia or cognitive decline such as dementia or cognitive impairment. A, B, X, R1, R2, R3 have meanings given in the description.

1,2,4 -TRIAZOLES AS ALLOSTERIC MODULATORS OF MGLU5 RECEPTOR ACTIVITY FOR THE TREATMENT OF SCHIZOPHRENIA OF DEMENTIA

-

, (2013/06/27)

This invention relates to compounds of formula (I) their use as positive allosteric modulators of mGlu5 receptor activity, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of neurological and psychiatric disorders associated with glutamate dysfunction such as schizophrenia or cognitive decline such as dementia or cognitive impairment. A, B, X, R1, R2, R3 have meanings given in the description.

COMPOUNDS FOR TREATING DISORDERS MEDIATED BY METABOTROPIC GLUTAMATE RECEPTOR 5, AND METHODS OF USE THEREOF

-

Page/Page column 157-158, (2010/11/03)

Provided herein are compounds and methods of synthesis thereof. The compounds provided herein are useful for the treatment, prevention, and/or management of various disorders, such as neurological disorders, psychiatric disorders, neuromuscular disorders, gastrointestinal disorders, lower urinary tract disorder, and cancer. Compounds provided herein modulate the activity of metabotropic glutamate receptor 5 (mGluR5) in the central nervous system or the periphery. Pharmaceutical formulations containing the compounds and their methods of use are also provided herein.

Parallel synthesis of substituted imidazoles from 1,2-aminoalcohols

Bleicher, Konrad H.,Gerber, Fernand,Wüthrich, Yves,Alanine, Alexander,Capretta, Alfredo

, p. 7687 - 7690 (2007/10/03)

Substituted imidazoles can be prepared efficiently from cyclic or acyclic 1,2-aminoalcohols via a four-step procedure involving acylation of the amine, oxidation of the alcohol, imine formation and cyclization. Examples are presented and the methodology i

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