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CAS

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1312425-07-2

1,2,3,4-Tetrahydrocyclopenta[b]indol-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1312425-07-2 Structure

  • Basic information

    1. Product Name: 1,2,3,4-Tetrahydrocyclopenta[b]indol-2-amine
    2. Synonyms: 1,3-Benzenedicarboxylic acid, 5-amino-, 1-ethyl ester
    3. CAS NO:1312425-07-2
    4. Molecular Formula: C10H11NO4
    5. Molecular Weight: 172.22638
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1312425-07-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 442.4±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.318±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
    8. Solubility: N/A
    9. PKA: 3.99±0.10(Predicted)
    10. CAS DataBase Reference: 1,2,3,4-Tetrahydrocyclopenta[b]indol-2-amine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,2,3,4-Tetrahydrocyclopenta[b]indol-2-amine(1312425-07-2)
    12. EPA Substance Registry System: 1,2,3,4-Tetrahydrocyclopenta[b]indol-2-amine(1312425-07-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1312425-07-2(Hazardous Substances Data)

1312425-07-2 Usage

Heterocyclic amine

A compound containing a cyclopentane ring fused to an indole ring This describes the structure of 1,2,3,4-Tetrahydrocyclopenta[b]indol-2-amine, which consists of a five-membered ring with two nitrogen atoms (amine group) attached to an indole ring.

Organic synthesis and pharmaceutical research

Building block for various biologically active molecules 1,2,3,4-Tetrahydrocyclopenta[b]indol-2-amine is used as a starting material in the creation of other compounds with potential biological activity, making it valuable in the development of new drugs and therapeutic agents.

Potential treatment for neurological and psychiatric disorders

The compound has been investigated for its possible use in treating various conditions related to the brain and nervous system, as well as mental health issues.

Analgesic and anti-inflammatory properties

1,2,3,4-Tetrahydrocyclopenta[b]indol-2-amine has been studied for its potential to relieve pain (analgesic) and reduce inflammation (anti-inflammatory), which could make it useful in the treatment of various conditions causing pain and swelling.

Serotonin 5-HT2A receptor antagonist

The compound is known for its ability to potentially block or inhibit the action of serotonin at the 5-HT2A receptor, a type of serotonin receptor involved in various physiological processes.

Study of serotonin receptor function and drug development

As a serotonin 5-HT2A receptor antagonist, 1,2,3,4-Tetrahydrocyclopenta[b]indol-2-amine serves as a valuable tool in researching the function of serotonin receptors and the development of drugs targeting these receptors for therapeutic purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 1312425-07-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,4,2 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1312425-07:
(9*1)+(8*3)+(7*1)+(6*2)+(5*4)+(4*2)+(3*5)+(2*0)+(1*7)=102
102 % 10 = 2
So 1312425-07-2 is a valid CAS Registry Number.

1312425-07-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-5-ethoxycarbonylbenzoic acid

1.2 Other means of identification

Product number -
Other names 3-Amino-5-(ethoxycarbonyl)benzoic 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:1312425-07-2 SDS

1312425-07-2Relevant articles and documents

SMALL MOLECULES THAT COVALENTLY MODIFY TRANSTHYRETIN

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Page/Page column 119-120, (2011/07/07)

A family of covalent kinetic stabilizer compounds that selectively and covalently react with the prominent plasma protein transthyretin in preference to more than 4000 other human plasma proteins is disclosed. A contemplated compound corresponds in struct

A stilbene that binds selectively to transthyretin in cells and remains dark until it undergoes a chemoselective reaction to create a bright blue fluorescent conjugate

Choi, Sungwook,Ong, Derrick Sek Tong,Kelly, Jeffery W.

supporting information; experimental part, p. 16043 - 16051 (2011/02/16)

We describe a non-fluorescent, second generation stilbene that very selectively binds to transthyretin in complex biological environments and remains dark until it chemoselectively reacts with the pKa-perturbed Lys-15 ε-amino group of transthyr

PIPERAZINYL COMPOUNDS

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Page/Page column 28-29, (2010/11/23)

A compound of formula (I) or a pharmaceutically acceptable salt thereof: [wherein Ar is aryl or heteroaryl, optionally substituted; R1 is acyl; R2 is H or lower alkyl; R3 is H, and the like; R4 is H, and the like.] having the activity inhibiting DPP-IV ac

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