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

61396-73-4

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61396-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61396-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,9 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61396-73:
(7*6)+(6*1)+(5*3)+(4*9)+(3*6)+(2*7)+(1*3)=134
134 % 10 = 4
So 61396-73-4 is a valid CAS Registry Number.

61396-73-4SDS

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 3-(4-fluorophenyl)propane-1,2-diol

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:61396-73-4 SDS

61396-73-4Upstream product

61396-73-4Downstream Products

61396-73-4Relevant academic research and scientific papers

Lewis Base Catalyzed Dioxygenation of Olefins with Hypervalent Iodine Reagents

Pan, Liangkun,Ke, Zhihai,Yeung, Ying-Yeung

supporting information, p. 8174 - 8178 (2021/10/25)

1,2-Diols are extremely useful building blocks in organic synthesis. Hypervalent iodine reagents are useful for the vicinal dihydroxylation of olefins to give 1,2-diols under metal-free conditions, but strongly acidic promoters are often required. Herein, we report a catalytic vicinal dioxygenation of olefins with hypervalent iodine reagents using Lewis bases as catalysts. The conditions are mild and compatible with various functional groups.

INHIBITORS OF JANUS KINASES

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Page/Page column 44, (2010/01/12)

The instant invention provides for compounds that inhibit the four known mammalian JAK kinases (JAK1, JAK2, JAK3 and TYK2) and PDK1. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting the activity of JAK1, JAK2, JAK3, TYK2 and PDK1 by administering the compound to a patient in need of treatment for myeloproliferative disorders or cancer.

INHIBITORS OF JANUS KINASES

-

Page/Page column 78, (2009/01/23)

The instant invention provides for compounds that inhibit the four known mammalian JAK kinases (JAK1, JAK2, JAK3 and TYK2) and PDK1. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting the activity of JAK1, JAK2, JAK3 TYK2 and PDK1 by administering the compound to a patient in need of treatment for myeloproliferative disorders or cancer.

1-(2-Ar-4-R-1,3-dioxolan-2-ylmethyl)imidazoles

-

, (2008/06/13)

1-(2-Ar-4-R-1,3-dioxolan-2-ylmethyl)imidazoles, useful as antifungal and antibacterial agents.

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