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96184-81-5

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96184-81-5 Usage

General Description

4-OXO-CYCLOHEXANECARBOXALDEHYDE is a chemical compound with the molecular formula C7H10O2. It is a cyclic aldehyde with a six-membered ring structure and a carbonyl group. 4-OXO-CYCLOHEXANECARBOXALDEHYDE is used in organic synthesis as a building block for the manufacture of various pharmaceuticals, dyes, and perfumes. It is also used as a precursor in the production of insecticides and herbicides. 4-OXO-CYCLOHEXANECARBOXALDEHYDE has potential applications in the field of medicine and agrochemicals due to its unique chemical properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 96184-81-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,8 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 96184-81:
(7*9)+(6*6)+(5*1)+(4*8)+(3*4)+(2*8)+(1*1)=165
165 % 10 = 5
So 96184-81-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O2/c8-5-6-1-3-7(9)4-2-6/h5-6H,1-4H2

96184-81-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclohexanone-4-carboxaldehyde

1.2 Other means of identification

Product number -
Other names 4-Oxo-cyclohexancarbaldehyd

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:96184-81-5 SDS

96184-81-5Relevant articles and documents

Stereoselective total synthesis of (±)-vindeburnol and (±)-16-epi-vindeburnol

Chen, Fener,Chen, Xiangtao,Tang, Pei,Wang, Huijing,Yu, Lei,Zhang, Wen

supporting information, p. 11669 - 11672 (2021/11/12)

A concise stereoselective total synthesis of (±)-vindeburnol and its epimer (±)-16-epi-vindeburnol is presented. This synthetic work features the utilization of Baeyer-Villiger oxidation to install different types of lactone substrate, and a sequence of a

FURANONE COMPOUNDS AND METHODS OF MAKING AND USING THE SAME

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Page/Page column 50, (2008/12/07)

The invention features compounds of the general Formula (I): (formula should be inserted here) Compounds of Formula (I) possess unexpectedly high affinity for Alk5 and/or Alk4, and can be useful as antagonists thereof for preventing and/or treating numerous diseases, including fibrotic disorders.

COMPOUND CONTAINING BASIC GROUP AND USE THEREOF

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Page/Page column 79-80, (2008/12/06)

The present invention relates to a compound represented by formula (I): wherein all symbols are as defined here, a salt thereof, a solvate thereof, or a prodrug thereof. The compound of the present invention has an antagonistic activity against CXCR4 and is therefore useful as a preventive and/or therapeutic agent for CXCR4-mediated diseases, for example, inflammatory and immune diseases (for example, rheumatoid arthritis, arthritis, retinopathy, pulmonary fibrosis, rejection of transplanted organ, etc.), allergic diseases, infections (for example, human immunodeficiency virus infection, acquired immunodeficiency syndrome, etc.), psychoneurotic diseases, cerebral diseases, cardiovascular disease, metabolic diseases, and cancerous diseases (for example, cancer, cancer metastasis, etc.), or an agent for regeneration therapy.

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