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(2-methyl-1-naphthyl)acetic acid, also known as 2M1NAA, is a synthetic compound that belongs to the family of naphthylacetic acids. It is known for its potential biological and pharmacological applications, including anti-inflammatory and anti-tumor activities. As a derivative of 1-naphthylacetic acid, 2M1NAA is thought to have similar properties and may act as a growth regulator in plants and a modulator of immune responses in animals.

85-08-5

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85-08-5 Usage

Uses

Used in Pharmaceutical Industry:
(2-methyl-1-naphthyl)acetic acid is used as a pharmaceutical agent for its potential anti-inflammatory and anti-tumor properties. It may be employed in the development of drugs targeting inflammation and cancer treatment.
Used in Agricultural Industry:
(2-methyl-1-naphthyl)acetic acid is used as a growth regulator in plants, potentially enhancing crop yield and quality. Its application in agriculture may contribute to more efficient and sustainable farming practices.
Further research is needed to fully understand the uses and effects of (2-methyl-1-naphthyl)acetic acid in various fields, including medicine and agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 85-08-5 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85-08:
(4*8)+(3*5)+(2*0)+(1*8)=55
55 % 10 = 5
So 85-08-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O2/c1-9-6-7-10-4-2-3-5-11(10)12(9)8-13(14)15/h2-7H,8H2,1H3,(H,14,15)

85-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methylnaphthalen-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-Methyl-1-naphthaleneacetic acid

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:85-08-5 SDS

85-08-5Downstream Products

85-08-5Relevant academic research and scientific papers

Aromatic Claisen Rearrangements of Benzyl Ketene Acetals: Conversion of Benzylic Alcohols to (ortho-Tolyl)acetates

Burns, Jed M.,Krenske, Elizabeth H.,McGeary, Ross P.

, p. 252 - 256 (2017/01/24)

Claisen rearrangements of benzyl vinyl ethers are much less facile than those of aliphatic allyl vinyl ethers, and their synthetic utility has remained relatively unexplored. A one-pot procedure is reported for the generation and Claisen rearrangement of benzyl vinyl ethers that contain an activating α-alkoxy substituent on the vinyl group. A [3,3]-sigmatropic mechanism was supported by trapping of the intermediate isotoluene in an intramolecular Alder–ene reaction.

Arylsulfonamide ethers, and methods of use thereof

-

, (2008/06/13)

Novel arylsulfonamide ether compounds and pharmaceutical compositions thereof are described. The use of the novel arylsulfonamide ether compounds and pharmaceutical compositions thereof as inhibitors of interleukin-1β converting enzyme and other cysteine proteases in the ICE family is also decribed. In addition, methods of treating stroke, inflammatory diseases, septic shock, repurfusion injury, Alzheimer's disease, and shigellosis using a compound of the invention or a pharmaceutical composition thereof are described.

Src family SH2 domain inhibitors

-

, (2008/06/13)

This invention relates to compounds of formula (1): wherein Ring a, A, B, C, D, E, R and Q are defined herein. These compounds possess the ability to disrupt the interaction between regulatory proteins possessing one or more SH2 domains and their native ligands.

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