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CarbaMic acid, N-[(1R)-3,3-dibroMo-1-Methyl-2-propen-1-yl]-, 1,1-diMethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 873009-27-9 Structure
  • Basic information

    1. Product Name: CarbaMic acid, N-[(1R)-3,3-dibroMo-1-Methyl-2-propen-1-yl]-, 1,1-diMethylethyl ester
    2. Synonyms: CarbaMic acid, N-[(1R)-3,3-dibroMo-1-Methyl-2-propen-1-yl]-, 1,1-diMethylethyl ester;(R)-tert-Butyl (4,4-dibromobut-3-en-2-yl)carbamate
    3. CAS NO:873009-27-9
    4. Molecular Formula: C9H15Br2NO2
    5. Molecular Weight: 329.0289
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 873009-27-9.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.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: CarbaMic acid, N-[(1R)-3,3-dibroMo-1-Methyl-2-propen-1-yl]-, 1,1-diMethylethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: CarbaMic acid, N-[(1R)-3,3-dibroMo-1-Methyl-2-propen-1-yl]-, 1,1-diMethylethyl ester(873009-27-9)
    11. EPA Substance Registry System: CarbaMic acid, N-[(1R)-3,3-dibroMo-1-Methyl-2-propen-1-yl]-, 1,1-diMethylethyl ester(873009-27-9)
  • 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: 873009-27-9(Hazardous Substances Data)

873009-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 873009-27-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,0,0 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 873009-27:
(8*8)+(7*7)+(6*3)+(5*0)+(4*0)+(3*9)+(2*2)+(1*7)=169
169 % 10 = 9
So 873009-27-9 is a valid CAS Registry Number.

873009-27-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[(2R)-4,4-dibromobut-3-en-2-yl]carbamate

1.2 Other means of identification

Product number -
Other names -

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:873009-27-9 SDS

873009-27-9Downstream Products

873009-27-9Relevant articles and documents

Heterocyclic Compounds Useful as RAF Kinase Inhibitors

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Page/Page column 43-44, (2009/01/24)

The present invention provides compounds useful as inhibitors of Raf protein kinase. The present invention also provides compositions thereof, and methods of treating Raf-mediated diseases.

COMPOUNDS USEFUL AS RAF KINASE INHIBITORS

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Page/Page column 87, (2009/03/07)

The present invention provides compounds useful as inhibitors of Raf protein kinase. The present invention also provides compositions thereof, and methods of treating Raf-mediated diseases.

MACROCYCLIC GHRELIN RECEPTOR MODULATORS AND METHODS OF USING THE SAME

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Page/Page column 40-41, (2008/12/07)

The present invention provides novel conformationally-defined macrocyclic compounds that can function as selective modulators of the ghrelin receptor (growth hormone secretagogue receptor, GHS-R1a and subtypes, isoforms and variants thereof). Methods of synthesizing the novel compounds are also described herein. These compounds are useful as agonists of the ghrelin receptor and as medicaments for treatment and prevention of a range of medical conditions including, but not limited to, metabolic and/or endocrine disorders, gastrointestinal disorders, cardiovascular disorders, obesity and obesity-associated disorders, central nervous system disorders, bone disorders, genetic disorders, hyperproliferative disorders and inflammatory disorders.

FACTOR XA INHIBITORS

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Page/Page column 95, (2008/06/13)

The present invention is directed to compounds represented by Formula I and pharmaceutically acceptable salts, solvates, hydrates, and prodrugs thereof which are inhibitors of Factor Xa. The present invention is also directed to and intermediates used in making such compounds, pharmaceutical compositions containing such compounds, methods to prevent or treat a number of conditions characterized by undesired thrombosis and methods of inhibiting the coagulation of a blood sample.

A new stereoselective synthesis of chiral γ-functionalized (E)-allylic amines

Reginato, Gianna,Mordini, Alessandro,Messina, Flavia,Degl'Innocenti, Alessandro,Poli, Giovanni

, p. 10985 - 10996 (2007/10/03)

Chiral t-Boc protected propargylic amines have been obtained starting from aminoaldehydes derived from natural aminoacids. Stannylcupration of these substrates affords an easy regio- and stereocontrolled route to the corresponding γ-stannylated (E)-allylamines which are useful intermediates for the synthesis of the corresponding γ-functionalized allylic systems.

Stereospecific synthesis of chiral alkinylogous amino acids

Reetz, Manfred T.,Strack, Thomas J.,Kanand, Juergen,Goddard, Richard

, p. 733 - 734 (2007/10/03)

tert-Butoxycarbonyl (Boc)-protected a-amino aldehydes, conventionally prepared from the corresponding (S)-α-amino acids, are converted via the Corey-Fuchs reaction into the N-protected alkinylogous amino acids, which on deprotection yield the correspondin

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