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CAS

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104605-95-0

1,2-Propanediol, 3-(4-fluorophenoxy)-, (2R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104605-95-0 Structure

  • Basic information

    1. Product Name: 1,2-Propanediol, 3-(4-fluorophenoxy)-, (2R)-
    2. Synonyms:
    3. CAS NO:104605-95-0
    4. Molecular Formula: C9H11FO3
    5. Molecular Weight: 186.183
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104605-95-0.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: 1,2-Propanediol, 3-(4-fluorophenoxy)-, (2R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Propanediol, 3-(4-fluorophenoxy)-, (2R)-(104605-95-0)
    11. EPA Substance Registry System: 1,2-Propanediol, 3-(4-fluorophenoxy)-, (2R)-(104605-95-0)

  • 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: 104605-95-0(Hazardous Substances Data)

104605-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104605-95-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,0 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104605-95:
(8*1)+(7*0)+(6*4)+(5*6)+(4*0)+(3*5)+(2*9)+(1*5)=100
100 % 10 = 0
So 104605-95-0 is a valid CAS Registry Number.

104605-95-0SDS

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 (2R)-1-(4-fluorophenoxy)propane-2,3-diol

1.2 Other means of identification

Product number -
Other names (-)-(R)-3-(4-fluorophenoxy)-1,2-propanediol

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:104605-95-0 SDS

104605-95-0Relevant articles and documents

Ring-conformer effects of the cyclopropyl group: First use of trans-(2r,3r)-cyclopropanecarbaldehydes as electrophiles in diastereoselective baylisihillman reaction

Krishna, Palakodety Radha,Kishore,Reddy, P. Srinivas

scheme or table, p. 2605 - 2608 (2010/03/03)

trans-(2R,3R)-Cyclopropanecarbaldehydes are used as novel electrophiles in the Baylis-Hillman reaction to afford adducts in good yields (75-85%) and diastereoselectivities (60-90%).

A novel and simple asymmetric synthesis of CMI-977 (LDP-977): A potent anti-asthmatic drug lead

Gurjar, Mukund K.,Murugaiah,Radhakrishna,Ramana,Chorghade, Mukund S.

, p. 1363 - 1370 (2007/10/03)

A practical gram scale asymmetric synthesis of CMI-977 is described. A tandem double elimination of an α-chlorooxirane and concomitant intramolecular nucleophilic substitution was used as the key step. Jacobsen hydrolytic kinetic resolution and Sharpless

Methods for synthesis of substituted tetrahydrofuran compound

-

, (2008/06/13)

The invention includes inter alia new methods for preparation of the pharmaceutically active compound 2-(4-fluorophenoxymethyl)-5-(4-N-hydroxyureidyl-1-butynyl)-tetrahydrofuran and precursors thereof.

Substituted oxygen alicyclic compounds, including methods for synthesis thereof

-

, (2008/06/13)

The invention provides new methods for preparation of cyclic oxygen compounds, including 2,5-disubstituted tetahydrofurans, 2,6-disubstituted tetrahydropyrans, 2,7-disubstituted oxepanes and 2,8-oxocanes. The invention also provides new cyclic oxygen compounds and pharmaceutical compositions and therapeutic methods that comprise such compounds.

Kinetic resolution of aryl glycidyl ethers : A practical synthesis of optically pure β-blocker - S-metoprolol

Gurjar, Mukund K.,Sadalapure, Kashinath,Adhikari, Susanta,Sarma, Bugga V. N. B. S.,Talukdar, Arindam,Chorghade, Mukund S.

, p. 1471 - 1476 (2007/10/03)

Kinetic resolution of (±)-aryl glycidyl ethers using (R,R)-salen Co(III)OAc and water provided enantiomerically pure arylglycidyl ether and 1-arylglycerol derivatives with high enantiomeric excess. Application of this approach to (S)-metoprolol has been d

Intermediates for the synthesis of benzoxazol- and benzothiazolamine derivatives, useful as anti-anoxic agents

-

, (2008/06/13)

Benzoxazol- and benzothiazolamine derivatives having anti-anoxic properties which compounds are useful in the treatment of anoxia. These compounds are produced from certain benzoxazol- and benzothizolamine intermediates.

Benzoxazol-and benzothiazolamine derivatives, useful as anti-anoxic agents

-

, (2008/06/13)

Benzoxazol-and benzothiazolamine derivatives having anti-anoxic properties which compounds are useful in the treatment of anoxia.

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