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1589-24-8

2-Oxocycloheptanecarbaldehyde is a chemical compound with the molecular formula C8H12O2. It is a cyclic ketone with a carbonyl group (C=O) and an aldehyde group (CHO) attached to a seven-membered ring. 2-oxocycloheptanecarbaldehyde is known for its unique structure, which contributes to its chemical properties and potential applications in various fields, such as pharmaceuticals and fragrances. Due to its cyclic nature and functional groups, 2-oxocycloheptanecarbaldehyde can participate in various chemical reactions, including nucleophilic addition, oxidation, and reduction. Its structure also makes it a potential precursor for the synthesis of more complex molecules.

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  • 1589-24-8 Structure

  • Basic information

    1. Product Name: 2-oxocycloheptanecarbaldehyde
    2. Synonyms: 2-oxocycloheptanecarbaldehyde;2-OXOCYCLOHEPTANE-1-CARBALDEHYDE(WXG02321)
    3. CAS NO:1589-24-8
    4. Molecular Formula: C8H12O2
    5. Molecular Weight: 140.17968
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1589-24-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 58-60 °C(Press: 1.5 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.101±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 7.08±0.20(Predicted)
    10. CAS DataBase Reference: 2-oxocycloheptanecarbaldehyde(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-oxocycloheptanecarbaldehyde(1589-24-8)
    12. EPA Substance Registry System: 2-oxocycloheptanecarbaldehyde(1589-24-8)

  • 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: 1589-24-8(Hazardous Substances Data)

1589-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1589-24-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,8 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1589-24:
(6*1)+(5*5)+(4*8)+(3*9)+(2*2)+(1*4)=98
98 % 10 = 8
So 1589-24-8 is a valid CAS Registry Number.

1589-24-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxocycloheptane-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-oxo-cycloheptanecarbaldehyde

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:1589-24-8 SDS

1589-24-8Relevant articles and documents

Synthetic Studies toward the Berkeleyacetal Core Architecture

Márquez-Cadena, Miguel Adrián,Zhang, Wei,Tong, Rongbiao

supporting information, p. 9227 - 9231 (2021/11/30)

Berkeleyacetals are structurally complex natural products that have shown potent anti-inflammatory activity. The presence of a highly dense oxygen functionality and a polycyclic ring system presents significant synthetic challenges. Herein, we report an e

CYCLOHEPTA(b)PYRIDINE-3-CARBONYLGUANIDINE DERIVATIVE AND PHARMACEUTICAL PRODUCT CONTAINING SAME

-

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

The present invention relates to a medicine, particularly a medicine comprising a novel cyclohepta[b]pyridine-3-carbonylguanidine derivative having an inhibitory effect on an Na+/H+ exchanger (NHE). There is provided a cyclohepta[b]p

REGIOSPECIFIC SYNTHESIS OF α-(PHENYLTHIO)CYCLOALKENONES AND OF α-PHENYL-α-(PHENYLTHIO)KETONES VIA αα-ADDITION OF PHENYLSULPHENYL CHLORIDE TO α-DIAZOKETONES

McKervey, M. Anthony,Ratananukul, Piniti

, p. 117 - 120 (2007/10/02)

Cyclic α-diazoketones react with phenylsulphenyl chloride at room temperature to furnish α-chloro-α-(phenylthio)cycloalkanones which undergo ready dehydrochlorination to α-(phenylthio)cycloalkenones when treated with triethylamine; acyclic, terminal α-diazoketones also furnish α-chloro-α-(phenylthio)adducts which are useful electrophiles in the synthesis of α-phenyl-α-(phenylthio)ketones.

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