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1-AMINO-6,7,8,9-TETRAHYDRO-5H-BENZO[7]ANNULEN-5-ONE is a heterocyclic chemical compound with the molecular formula C13H13NO. It features a benzene ring fused to a cycloheptene ring, with a ketone and an amino group attached to the benzene ring. 1-AMINO-6,7,8,9-TETRAHYDRO-5H-BENZO[7]ANNULEN-5-ONE has potential applications in the pharmaceutical industry, particularly in the development of new drugs and medications. Careful handling is advised due to potential hazards and risks associated with its use and handling.
Used in Pharmaceutical Industry:
1-AMINO-6,7,8,9-TETRAHYDRO-5H-BENZO[7]ANNULEN-5-ONE is used as a key intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique structure allows for the development of new drugs and medications that can address specific medical needs.

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  • 870679-59-7 Structure
  • Basic information

    1. Product Name: 1-AMINO-6,7,8,9-TETRAHYDRO-5H-BENZO[7]ANNULEN-5-ONE
    2. Synonyms: 1-AMINO-6,7,8,9-TETRAHYDRO-5H-BENZO[7]ANNULEN-5-ONE;5H-Benzocyclohepten-5-one, 1-aMino-6,7,8,9-tetrahydro-
    3. CAS NO:870679-59-7
    4. Molecular Formula: C11H13NO
    5. Molecular Weight: 175.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 870679-59-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 93-95 °C(Press: 0.05 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.146±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: 3.24±0.20(Predicted)
    10. CAS DataBase Reference: 1-AMINO-6,7,8,9-TETRAHYDRO-5H-BENZO[7]ANNULEN-5-ONE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-AMINO-6,7,8,9-TETRAHYDRO-5H-BENZO[7]ANNULEN-5-ONE(870679-59-7)
    12. EPA Substance Registry System: 1-AMINO-6,7,8,9-TETRAHYDRO-5H-BENZO[7]ANNULEN-5-ONE(870679-59-7)
  • 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: 870679-59-7(Hazardous Substances Data)

870679-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 870679-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,6,7 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 870679-59:
(8*8)+(7*7)+(6*0)+(5*6)+(4*7)+(3*9)+(2*5)+(1*9)=217
217 % 10 = 7
So 870679-59-7 is a valid CAS Registry Number.

870679-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-amino-6,7,8,9-tetrahydrobenzo[7]annulen-5-one

1.2 Other means of identification

Product number -
Other names 5H-Benzocyclohepten-5-one,1-amino-6,7,8,9-tetrahydro

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:870679-59-7 SDS

870679-59-7Relevant articles and documents

Vinyl Carbocations Generated under Basic Conditions and Their Intramolecular C-H Insertion Reactions

Wigman, Benjamin,Popov, Stasik,Bagdasarian, Alex L.,Shao, Brian,Benton, Tyler R.,Williams, Chloé G.,Fisher, Steven P.,Lavallo, Vincent,Houk,Nelson, Hosea M.

supporting information, p. 9140 - 9144 (2019/06/08)

Here we report the surprising discovery that high-energy vinyl carbocations can be generated under strongly basic conditions, and that they engage in intramolecular sp3 C-H insertion reactions through the catalysis of weakly coordinating anion salts. This approach relies on the unconventional combination of lithium hexamethyldisilazide base and the commercially available catalyst, triphenylmethylium tetrakis(pentafluorophenyl)borate. These reagents form a catalytically active lithium species that enables the application of vinyl cation C-H insertion reactions to heteroatom-containing substrates.

Tricyclic pyrazoles. 3. Synthesis, biological evaluation, and molecular modeling of analogues of the cannabinoid antagonist 8-chloro-1-(2′, 4′-dichlorophenyl)-N-piperidin-1-yl-1,4,5,6-tetrahydrobenzo[6,7] cyclohepta[1,2-c]pyrazole-3-carboxamide

Murineddu, Gabriele,Ruiu, Stefania,Loriga, Giovanni,Manca, Ilaria,Lazzari, Paolo,Reali, Roberta,Pani, Luca,Toma, Lucio,Pinna, Gérard A.

, p. 7351 - 7362 (2007/10/03)

A series of analogues of 8-chloro-1-(2′,4′-dichlorophenyl)-AT- piperidin-1-yl-1,4,5,6-tetrahydrobenzo-[6,7]cyclohepta[1,2-c] pyrazole-3-carboxamide 4a (NESS 0327) (Ruiu, S.; Pinna, G. A.; Marchese, G.; Mussinu, J. M.; Saba, P.; Tambaro, S.; Casti, P.; Var

Substituted guanidine derivatives and process for producing the same

-

Page column 58, (2010/01/31)

A compound represented by the general formula (1): wherein each of R1, R2, R3, R4and R5is a hydrogen atom, an alkyl group, a substituted alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, a cycloalkenyl group, a saturated heterocyclic group, an aromatic group, an acyl group or the like; each of Y1, Y2, Y3and Y4is a single bond, —CH2—, —O—, —CO— or the like, provided that at least two of Y1through Y4are independently a group other than a single bond; and Z may be absent, or one or more Zs may be present and are independently an alkyl group, a substituted alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, a cycloalkenyl group, a saturated heterocyclic group, a halogen atom, a carboxyl group, an alkoxycarbonyl group, an aromatic group, an acyl group or the like, is useful as a therapeutic or prophylactic agent for diseases caused by the acceleration of the sodium/proton exchange transport system.

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