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1,4-Methanonaphthalene-2-carboxylicacid,2-amino-1,2,3,4-tetrahydro-,(1alpha,2beta,4alpha)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91733-74-3

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91733-74-3 Usage

Explanation

This is the full systematic name of the compound, which describes its structure and stereochemistry.

Explanation

The molecular formula represents the number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms in the compound.

Explanation

The compound is derived from naphthalene, a fused ring system consisting of two benzene rings. It has a carboxylic acid (-COOH) and an amino group (-NH2) attached to the ring.

Explanation

The compound is classified as a cycloalkane carboxylic acid due to the presence of a carboxylic acid functional group attached to a cyclic hydrocarbon.

Explanation

The compound is commonly used in pharmaceutical research and drug development due to its unique molecular structure and reactivity.

Explanation

The compound may have potential applications in the fields of organic synthesis and medicinal chemistry, although further research is needed to fully understand its potential uses and effects.

Explanation

The stereochemistry of the compound is described by the (1alpha,2beta,4alpha)-(9CI) notation, which indicates the spatial arrangement of the atoms in the molecule.

Explanation

The compound is considered a complex organic compound due to its multiple functional groups and the fusion of two benzene rings in its structure.

Explanation

Additional research is required to explore the compound's potential applications, reactivity, and effects in various fields, such as pharmaceuticals and organic synthesis.

Structure

Derivative of naphthalene with a carboxylic acid and an amino group attached to the ring structure

Type

Cycloalkane carboxylic acid

Applications

Pharmaceutical research and drug development

Potential Applications

Organic synthesis and medicinal chemistry

Stereochemistry

(1alpha,2beta,4alpha)-(9CI)

Complexity

Complex organic compound

Further Research

Needed to fully understand potential uses and effects

Check Digit Verification of cas no

The CAS Registry Mumber 91733-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,3 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91733-74:
(7*9)+(6*1)+(5*7)+(4*3)+(3*3)+(2*7)+(1*4)=143
143 % 10 = 3
So 91733-74-3 is a valid CAS Registry Number.

91733-74-3SDS

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 2-endo-amino-1,2,3,4-tetrahydro-1,4-methanonaphthalene-2-exo-carboxylic acid

1.2 Other means of identification

Product number -
Other names endo-2-aminobenzonorbornen-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:91733-74-3 SDS

91733-74-3Downstream Products

91733-74-3Relevant academic research and scientific papers

Synthesis and Stereochemical Analysis of 2-Amino-1,2,3,4-tetrahydro-1,4-methanonaphthalene-2-carboxylic Acid, A Conformationally Rigid Phenylalanine Derivative

Layton, John W.,Smith, Stanford L.,Crooks, Peter A.,Deeks, Trevor,Waigh, Roger D.

, p. 1283 - 1287 (2007/10/02)

A rigid phenylalanine analogue, 2-amino-1,2,3,4-tetrahydro-1,4-methanonaphthalene-2-carboxylic acid (3) of unknown stereochemistry was obtained as the sole amino acid product from a Strecker reaction with 1,2,3,4-tetrahydro-1,4-methanonaphthalen-2-one (4)

Leucine enkephalin analogues containing a conformationally restained N-terminal amino acid residue

Deeks,Crooks,Waigh

, p. 457 - 460 (2007/10/02)

Three analogues of leucine enkephalin, in which the terminal tyrosine-1 residue has been replaced by conformationally restrained aromatic amino acids, have been synthesized by classical solution methods. Their opiate agonist potencies on electrically stimulated guinea pig ileum and mouse vas deferens preparations were determined and compared with morphine, metenkephalin, and Leu enkephalin. None of these analogues had analgesic properties when evaluated on the above tissue preparations or when evaluated by the hot-plate test in mice after subcutaneous and intracerebroventricular administration.

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