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4-Methoxy-2,3-dihydro-1H-indene-2-carboxylic acid is a chemical compound with a molecular formula C12H12O3. It is a derivative of indene carboxylic acid, characterized by the presence of a methoxy group and a carboxylic acid group in its structure. 4-Methoxy-2,3-dihydro-1H-indene-2-carboxylic acid is known for its potential biological activities and is commonly used in the synthesis of pharmaceuticals and other organic compounds, making it a versatile compound with applications in the pharmaceutical and chemical industries.

76413-91-7

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76413-91-7 Usage

Uses

Used in Pharmaceutical Synthesis:
4-Methoxy-2,3-dihydro-1H-indene-2-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Organic Synthesis:
4-Methoxy-2,3-dihydro-1H-indene-2-carboxylic acid is used as a building block in organic synthesis, enabling the creation of a wide range of organic compounds for various applications, including the development of new materials and chemicals.
Used in Medicinal Chemistry:
4-Methoxy-2,3-dihydro-1H-indene-2-carboxylic acid is used as a starting material in medicinal chemistry, where it can be further modified to explore its potential biological activities and develop new therapeutic agents.
Used in Drug Discovery:
Due to its potential biological activities, 4-Methoxy-2,3-dihydro-1H-indene-2-carboxylic acid is used in drug discovery processes to identify and optimize new drug candidates for the treatment of various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 76413-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,1 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76413-91:
(7*7)+(6*6)+(5*4)+(4*1)+(3*3)+(2*9)+(1*1)=137
137 % 10 = 7
So 76413-91-7 is a valid CAS Registry Number.

76413-91-7SDS

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 4-Methoxy-2,3-dihydro-1H-indene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-methoxy-2,3-dihydro-1H-indene-2-carboxylic 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:76413-91-7 SDS

76413-91-7Downstream Products

76413-91-7Relevant academic research and scientific papers

Monophenolic 2-(dipropylamino)indans and related compounds: Central dopamine-receptor stimulating activity

Hacksell,Arvidsson,Svensson,Nilsson,Wikstroem,Lindberg,Sanchez,Hjorth,Carlsson,Paalzow

, p. 429 - 434 (2007/10/02)

Monophenolic 2-(dipropylamino)indans and related compounds have been synthesized and tested for central dopamine-receptor stimulating activity, using biochemical and behavioral tests in rats and emesis tests in dogs. The active compounds possess similar relative potencies in eliciting the three different dopamine-receptor mediated effects measured. 4-Hydroxy-2-(dipropylamino)indan was the most potent of the new compounds. The corresponding 5-hydroxy analogue was less active. 4-Hydroxy-2-[(dipropylamino)methyl]indan is a new type of dopaminergic agent with a phenylpropylamine moiety in its framework instead of the phenylethylamine structure, common to most dopamine-receptor agonists. This compound was 10-20 times less active than apomorphine. 6,7,8,9-Tetrahydro-1-hydroxy-N,N-dipropyl-5H-6-benzocycloheptenylamine-5-hydroxy-2-[(dipropylamino)methyl]tetralin were both inactive. Since the intramolecular distances between functional groups in the indans studied here are different from those in, for example, apomorphine, it is concluded that a certain variation of these distances can be accepted by the receptor. It could also be demonstrated that the position of the OH group on the aromatic ring is of importance for the activity and that emetic activity may be associated with dopaminergic agonists of the indan as well as of the tetralin type of structure.

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