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18709-01-8

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18709-01-8 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 50, p. 4877, 1985 DOI: 10.1021/jo00224a045

Check Digit Verification of cas no

The CAS Registry Mumber 18709-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,0 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18709-01:
(7*1)+(6*8)+(5*7)+(4*0)+(3*9)+(2*0)+(1*1)=118
118 % 10 = 8
So 18709-01-8 is a valid CAS Registry Number.

18709-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxocyclohexane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names Cyclohexanon-(2)-carbonsaeure-(1)

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:18709-01-8 SDS

18709-01-8Relevant articles and documents

Application of copper(II)-mediated radical cross-dehydrogenative coupling to prepare spirocyclic oxindoles and to a formal total synthesis of Satavaptan

Hurst, Timothy E.,Gorman, Ryan,Drouhin, Pauline,Taylor, Richard J.K.

, p. 6485 - 6496 (2018)

Application of radical cross-dehydrogenative coupling (CDC) procedures to prepare a range of novel spirocyclic oxindoles and to a formal total synthesis of the vasopressin V2 receptor antagonist Satavaptan is reported. The key step involves a c

Mechanism of the Carboxylation of Cyclohexanone with Carbon Dioxide Catalyzed by 1,8-Diazabicycloundec-7-ene

Mori, Hisakazu

, p. 435 - 440 (1988)

The dependence of the rate of carboxylation upon the concentration of the reactant was investigated in dimethyl sulfoxide.The reaction rate depended upon the concentration of cyclohexanone and 1,8-diazabicycloundec-7-ene(DBU) in the first order, re

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Bottaccio,Chiusoli

, p. 618 (1966)

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Enantioselective Synthesis of Medium-Sized-Ring Lactones via Iridium-Catalyzed Z-Retentive Asymmetric Allylic Substitution Reaction

Ding, Lu,Song, Hao,Zheng, Chao,You, Shu-Li

supporting information, p. 4770 - 4775 (2022/03/27)

Medium-sized rings are important structural units, but their synthesis, especially in a highly enantioselective manner, has been a great challenge. Herein we report an enantioselective synthesis of medium-sized-ring lactones by an iridium-catalyzed Z-retentive asymmetric allylic substitution reaction. The reaction features mild conditions and a broad substrate scope. Various eight- to 11-membered-ring lactones can be afforded in moderate to excellent yields (up to 88%) and excellent enantioselectivity (up to 99% ee). The utilization of both Z-allyl precursors and an Ir catalyst is critical for the medium-sized-ring formation.

Amide derivative, preparation method of amide derivative, and application of amide derivative to pharmacy

-

Paragraph 0250-0253, (2017/08/30)

The invention provides an amide derivative, a preparation method of the amide derivative, and application of the amide derivative to pharmacy. The amide derivative compound is selected from one of the following structures. The compound can be used for preparing medicines in the fields of local anaesthesia or analgesia. (The formulas are as shown in the description).

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