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8-Amino-3,4-dihydro-1H-naphthalen-2-one, also known as 2-amino-1-tetralone, is a chemical compound with the molecular formula C11H11NO. It is an amino derivative of tetralone, a bicyclic compound, and is valued as a building block in the synthesis of various pharmaceuticals and organic compounds. This white to yellow solid has a melting point of approximately 130-132°C and can be synthesized through the reduction of 2-nitro-1-tetralone or the corresponding ketone.

624729-74-4

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624729-74-4 Usage

Uses

Used in Pharmaceutical Industry:
8-Amino-3,4-dihydro-1H-naphthalen-2-one is used as an intermediate in the production of various pharmaceuticals for its ability to be a key component in the synthesis of medicinal compounds.
Used in Organic Chemistry:
8-Amino-3,4-dihydro-1H-naphthalen-2-one is used as a valuable building block in organic chemistry for its versatility in forming other chemical compounds, contributing to the development of new materials and substances.

Check Digit Verification of cas no

The CAS Registry Mumber 624729-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,4,7,2 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 624729-74:
(8*6)+(7*2)+(6*4)+(5*7)+(4*2)+(3*9)+(2*7)+(1*4)=174
174 % 10 = 4
So 624729-74-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO/c11-10-3-1-2-7-4-5-8(12)6-9(7)10/h1-3H,4-6,11H2

624729-74-4SDS

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 8-Amino-3,4-dihydro-1H-naphthalen-2-one

1.2 Other means of identification

Product number -
Other names 8-amino-3,4-dihydro-lH-naphthalen-2-one

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:624729-74-4 SDS

624729-74-4Relevant academic research and scientific papers

Tetrahydro-naphthols as orally available TRPV1 inhibitors

Urbahns, Klaus,Yura, Takeshi,Gupta, Jang B.,Tajimi, Masaomi,Fujishima, Hiroshi,Masuda, Tsutomu,Yamamoto, Noriyuki,Ikegami, Yuka,Marumo, Makiko,Yasoshima, Kayo,Yoshida, Nagahiro,Moriwaki, Toshiya,Madge, David,Chan, Fiona,Mogi, Muneto

scheme or table, p. 3408 - 3411 (2012/06/29)

Starting from a naphthol-based lead series with low oral bioavailability, we have identified potent TRPV1 antagonists with oral bioavailability in rats. These compounds emerged from SAR studies aimed at replacing the lead's phenol structure whilst maintai

SUBSTITUTED AROMATIC CARBOXAMIDE AND UREA DERIVATIVES AS VANILLOID RECEPTOR LIGANDS

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Page/Page column 150, (2010/11/18)

The invention relates to substituted aromatic carboxamide and urea derivatives, to processes for the preparation thereof, to pharmaceutical compositions containing these compounds and also to the use of these compounds for preparing pharmaceutical compositions (formula (I)).

Vanilloid receptor (VR) inhibitors for treatment of Human Immunodeficiency Virus (HIV)-mediated pain states

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Page 11, (2008/06/13)

The invention relates to the application of Vanilloid receptor (VR) 1 inhibitors for drug development and for the treatment of HIV-mediated neuropathies and neuropathic pain states. Further, the inventor identified a novel signaling cascade connecting the

TETRAHYDRO-NAPHTHALENE AND UREA DERIVATIVES

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Page/Page column 100-101, (2015/05/06)

This invention relates to tetrahydro-naphthalene and urea derivatives and salts thereof which are useful as active ingredients of pharmaceutical preparations. The tetrahydro-naphthalene and urea derivatives of the present invention have vanilloid receptor (VR1) antagonistic activity, and can be used for the prophylaxis and treatment of diseases associated with VR1 activity, in particular for the treatment of urological diseases or disorders, such as detrusor overactivity (overactive bladder), urinary incontinence, neurogenic detrusor oeractivity (detrusor hyperflexia), idiopathic detrusor overactivity (detrusor instability), benign prostatic hyperplasia, and lower urinary tract symptoms; chronic pain, neuropathic pain, postoperative pain, rheumatoid arthritic pain, neuralgia, neuropathies, algesia, nerve injury, ischaemia, neurodegeneration, stroke, and inflammatory disorders such as asthma and chronic obstructive pulmonary (or airways) disease (COPD). BHC 03 2 001-Foreign-Countries - 66 - BHC 03 2 001-Foreign-Countries - 65 -

HYDROXY-TETRAHYDRO-NAPHTHALENYLUREA DERIVATIVES

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Page 41-42, (2008/06/13)

This invention relates to hydroxy-tetrahydro-naphthalenylurea derivatives and salts thereof which are useful as active ingredients of pharmaceutical preparations. The hydroxy-tetrahydro-naphthalenylurea derivatives of the present invention have an excelle

TETRAHYDRO-NAPHTHALENE DERIVATIVES AS VANILLOID RECEPTOR ANTAGONISTS

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Page 42-43, (2008/06/13)

This invention relates to tetrahydro-naphthalene derivatives and salts thereof which is useful as an active ingredient of pharmaceutical preparations. The tetrahydro-naphthalene derivatives of the present invention have an excellent activity as VR1 antago

TETRAHYDRO-NAPHTHALENE DERIVATIVES

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Page 51-52, (2010/02/07)

This invention relates to tetrahydro-naphthalene derivatives and salts thereof which is useful as an active ingredient of pharmaceutical preparations. The tetrahydro-naphthalene derivatives of the present invention have an excellent activity as VR1 antago

HYDROXY TETRAHYDRO-NAPHTHALENYLUREA DERIVATIVES

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Page/Page column 46, (2008/06/13)

This invention relates to tetrahydro-naphthalene derivatives and salts thereof which is useful as an active ingredient of pharmaceutical preparations. The tetrahydro-naphthalene derivatives of the present invention have an excellent activity as VR1 antago

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