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3-(1-ADAMANTYL)-3-OXOPROPANENITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23938-42-3

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23938-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23938-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,3 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23938-42:
(7*2)+(6*3)+(5*9)+(4*3)+(3*8)+(2*4)+(1*2)=123
123 % 10 = 3
So 23938-42-3 is a valid CAS Registry Number.

23938-42-3SDS

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 3-(1-ADAMANTYL)-3-OXOPROPANENITRILE

1.2 Other means of identification

Product number -
Other names Tricyclo[3.3.1.13,7]decane-1-propanenitrile, β-oxo-

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:23938-42-3 SDS

23938-42-3Relevant academic research and scientific papers

One-pot dichlorinative deamidation of primary β-ketoamides

Zheng, Congke,Zhang, Xiaohui,Ijaz Hussain, Muhammad,Huang, Mingming,Liu, Qing,Xiong, Yan,Zhu, Xiangming

, p. 574 - 577 (2017/01/16)

An approach to the dichlorinative deamidation of primary β-ketoamides through ketonic cleavage is described, and a series of α,α-dichloroketones were furnished mostly in the presence of TEMPO. Based on control experiments, a mechanism involving tandem dichlorination and deamidation is proposed to interpret the observed reactivity.

Reactions of methyl esters of adamantane acids with acetonitrile

Shiryaev,Belen′kaya,Shiryaev,Rybakov,Klimochkin, Yu. N.

, p. 2966 - 2969 (2016/09/28)

Methyl adamantane-1-carboxylate and methyl (1-adamantyl)acetate react with acetonitrile in the presence of sodium hydride to give 3-(1-adamantyl)-3-oxopropanenitrile and 4-(1-adamantyl)-3-oxobutanenitrile, respectively. Reaction involving methyl (1-adamantyl)-acetate produces also 2-(1-adamantyl)-N-(E-1-cyanoprop-1-ene-2-yl)acetamide; the structure of this side product was established by X-ray diffraction analysis.

P38 MAP KINASE INHIBITORS

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Page/Page column 54, (2011/10/31)

There is provided a compound of formula (I): wherein: J represents (A): or (B): compositions comprising same, processes for preparing said compounds and use thereof in treatment, particularly in the treatment of inflammatory disease, such as asthma, COPD and 15 rheumatoid arthritis.

Photographic material and process comprising a pyrazolotriazole coupler

-

, (2008/06/13)

Novel 1H-pyrazolo[1,5-b]1,2,4 triazole couplers containing in the 6- position an unsubstituted or substituted multicyclic hydrocarbon group, eg an adamantyl group, in a photographic material and process enable dye images that exhibit improved light stability. These couplers are useful in photographic materials and processes.

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