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2-allyl-3-acetamidophenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37439-79-5

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37439-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37439-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,4,3 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37439-79:
(7*3)+(6*7)+(5*4)+(4*3)+(3*9)+(2*7)+(1*9)=145
145 % 10 = 5
So 37439-79-5 is a valid CAS Registry Number.

37439-79-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-allyl-3-acetamidophenol

1.2 Other means of identification

Product number -
Other names N-(2-allyl-3-hydroxyphenyl)acetamide

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:37439-79-5 SDS

37439-79-5Relevant academic research and scientific papers

LEUKOTRIENE B4 ANTAGONIST COMPOUND

-

Page/Page column 9; 10, (2013/07/25)

The present invention provides a compound of Formula (I): or a pharmaceutically acceptable salt thereof. Also, the present invention provides a pharmaceutical composition comprising a compound of Formula (I) or a pharmaceutically acceptable salt thereof a

1-(PIPERIDIN-4-YL)-1H-INDOLE DERIVATIVE

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Page/Page column 34-35, (2010/11/28)

The present invention provides a compound represented by the formula (1) or a pharmacologically acceptable salt thereof, or a hydrate thereof (provided that a compound in which all of R4a, R4b, and R4c are hydrogen atoms is excluded.): [wherein R1 represents a hydrogen atom, R2 represents a hydrogen atom, R3 represents the formula: wherein R4a, R4b, and R4c are the same as or different from each other and each represents a hydrogen atom, a C1-6 alkyl group or a C1-6 alkoxy group, etc.]

Synthesis of 7-methoxybenzolactam-V8 using a diastereoselective Strecker synthesis

Sakamuri,Kozikowski

, p. 475 - 476 (2007/10/03)

7-Methoxybenzolactam-V8 (4) was synthesized using a diastereoselective Strecker reaction as the key step employing an ortho-substituted phenylacetaldehyde and (R)-phenylglycinol as the chiral auxiliary.

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