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(5Z)-N-(4-hydroxy-3-methoxybenzyl)-7-methyloct-5-enamide is a chemical compound with a molecular formula C20H29NO3. It is an amide compound, characterized by a carbonyl group (C=O) bonded to a nitrogen atom. The structure features a long hydrocarbon chain with a double bond and a hydroxyl group attached to a benzyl ring, which also contains a methoxy group, indicating the presence of a methyl group (-CH3) bonded to an oxygen atom. These structural elements make (5Z)-N-(4-hydroxy-3-methoxybenzyl)-7-methyloct-5-enamide a promising candidate for exploration in medicinal chemistry and pharmacology due to its potential biological activities and therapeutic applications.

112375-60-7

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112375-60-7 Usage

Uses

Used in Medicinal Chemistry:
(5Z)-N-(4-hydroxy-3-methoxybenzyl)-7-methyloct-5-enamide is used as a compound of interest in medicinal chemistry for its unique structural features, which may contribute to potential biological activities and therapeutic effects.
Used in Pharmacology Research:
In the field of pharmacology, (5Z)-N-(4-hydroxy-3-methoxybenzyl)-7-methyloct-5-enamide is utilized for studying its possible interactions with biological targets, which could lead to the development of new drugs or therapeutic agents.
Used in Drug Development:
(5Z)-N-(4-hydroxy-3-methoxybenzyl)-7-methyloct-5-enamide is considered in drug development as a potential lead compound. Its specific structural elements, including the amide bond, hydrocarbon chain, double bond, hydroxyl group, and methoxy group, may offer avenues for the creation of new medications with novel mechanisms of action.
Used in Chemical Synthesis:
(5Z)-N-(4-hydroxy-3-methoxybenzyl)-7-methyloct-5-enamide is also used in chemical synthesis processes, where its unique structure can be further modified or used as a building block to create new molecules with specific properties for various applications in the chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 112375-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,3,7 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112375-60:
(8*1)+(7*1)+(6*2)+(5*3)+(4*7)+(3*5)+(2*6)+(1*0)=97
97 % 10 = 7
So 112375-60-7 is a valid CAS Registry Number.

112375-60-7SDS

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 (Z)-N-[(4-hydroxy-3-methoxyphenyl)methyl]-7-methyloct-5-enamide

1.2 Other means of identification

Product number -
Other names (Z)-N-(4-hydroxy-3-methoxybenzyl)-7-methyloct-5-enamide

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:112375-60-7 SDS

112375-60-7Downstream Products

112375-60-7Relevant academic research and scientific papers

The Capsaicinoids: Their Separation, Synthesis, and Mutagenicity

Gannett, Peter M.,Nagel, Donald L.,Reilly, Pam J.,Lawson, Terence,Sharpe, Jody,Toth, Bela

, p. 1064 - 1071 (2007/10/02)

Capsaicin (1b), the pungent ingredient in many varietes of Capsicums has recently been implicated as a possible carcinogen.When obtained from natural sources 1b is always accompanied by a number of related homologues.We have isolated seven of these homologues, characterized them, and synthesized them by a general and unique route developed in our laboratories.Also reported are mutagenicity data for 1b and an extract of red pepper as measured by the Ames assay and the V-79 mammalian cell assay.

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