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4-fluoro-α-oxobenzenepropanoic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161038-68-2

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161038-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161038-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,0,3 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 161038-68:
(8*1)+(7*6)+(6*1)+(5*0)+(4*3)+(3*8)+(2*6)+(1*8)=112
112 % 10 = 2
So 161038-68-2 is a valid CAS Registry Number.

161038-68-2SDS

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 4-fluoro-α-oxobenzenepropanoic acid ethyl ester

1.2 Other means of identification

Product number -
Other names Ethyl 3-(4-fluorophenyl)-2-oxopropanoate

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:161038-68-2 SDS

161038-68-2Relevant academic research and scientific papers

ARGININE METHYLTRANSFERASE INHIBITORS AND USES THEREOF

-

, (2014/10/29)

Described herein are compounds of Formula (I), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting arginine methyltransferase activity. Methods of using the compo

Fused lactones as a route to functionalized 1-substituted indoles

Schuster,Coppola

, p. 1381 - 1384 (2007/10/02)

Indole lactones 8 and 14 were synthesized as a means of functionalizing the 1-isopropyl substituent of the indole nucleus. Lactone 8, upon reduction with diisobutylaluminum hydride, produces lactol 9 which behaves like a masked hydroxy aldehyde and underg

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