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Carbamic acid, ethyl(2-hydroxyethyl)-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 67249-24-5 Structure
  • Basic information

    1. Product Name: Carbamic acid, ethyl(2-hydroxyethyl)-, phenylmethyl ester
    2. Synonyms:
    3. CAS NO:67249-24-5
    4. Molecular Formula: C12H17NO3
    5. Molecular Weight: 223.272
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67249-24-5.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: Carbamic acid, ethyl(2-hydroxyethyl)-, phenylmethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, ethyl(2-hydroxyethyl)-, phenylmethyl ester(67249-24-5)
    11. EPA Substance Registry System: Carbamic acid, ethyl(2-hydroxyethyl)-, phenylmethyl ester(67249-24-5)
  • 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: 67249-24-5(Hazardous Substances Data)

67249-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67249-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,4 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67249-24:
(7*6)+(6*7)+(5*2)+(4*4)+(3*9)+(2*2)+(1*4)=145
145 % 10 = 5
So 67249-24-5 is a valid CAS Registry Number.

67249-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-ethyl N-(2-hydroxyethyl) carbamate

1.2 Other means of identification

Product number -
Other names N-benzyloxycarbonyl-N-ethyl-2-aminoethanol

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:67249-24-5 SDS

67249-24-5Relevant articles and documents

AMIDOETHYL AZOLE OREXIN RECEPTOR ANTAGONISTS

-

Page/Page column 34-35, (2016/07/27)

An amidoethyl azole compounds are provided as antagonists of orexin receptors. The compounds may be used for treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved.

CHEMICAL COMPOUNDS

-

Page/Page column 48, (2012/02/15)

The present invention relates to compounds of Formula (I): and to their salts, pharmaceutical compositions, methods of use, and methods for their preparation. These compounds inhibit Bcl-2 and/or Bcl-XL activities and may be used for the treatment of cancer.

Synthesis of two metabolites of the antiarrythmicum amiodarone

Wendt, Barbara,Ha, Huy Riem,Hesse, Manfred

, p. 2990 - 3001 (2007/10/03)

The metabolism of the potent antiarrythmic drug amiodarone (AMI; 1) has yet not been fully investigated. Recently, in vitro experiments revealed that in rabbit-liver microsomes, AMI (1) and its main metabolite MDEA (2) were biotransformed to the hydroxyla

SYNTHESIS AND USE OF BENZYL TERT-BUTYL IMINODICARBONATE, A VERSATILE REAGENT FOR THE PREPARATION OF AMINES

Grehn, Leif,Ragnarsson, Ulf

, p. 2778 - 2786 (2007/10/02)

An efficient synthesis of benzyl tert-butyl iminodicarbonate (IV), starting from benzoyl isocyanate, is reported.Reaction of the isocyanate with benzyl alcohol gave benzyl N-benzoylcarbamate (II) which on exhaustive tert-butoxycarbonylation via the non-isolated triacyl amine III, after aminolysis, provided the title compound.The sodium salt V was alkylated with various halides under Gabriel conditions to give in high yields the corresponding benzyloxycarbonyl tert-butoxycarbonyl diprotected amines.Similarly, compound IV was alkylated with alcohols under Mitsunobu conditions to give some additional amines of this type, from which the protecting groups can be removed selectively under mild conditions.

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