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3-Chloroadamantane-1-carboxylic acid is an organic compound that falls under the category of carboxylic acids and derivatives. It is distinguished by a molecular structure that includes a carboxyl group, a chloro substituent, and an adamantane, which is a dense, diamond-like, three-dimensional arrangement of carbon atoms. This unique framework makes it a subject of interest in organic chemistry and valuable for scientific research and pharmaceutical drug development.

34859-74-0

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34859-74-0 Usage

Uses

Used in Scientific Research:
3-Chloroadamantane-1-carboxylic acid is used as a research compound for its distinctive molecular structure and properties, contributing to the advancement of organic chemistry.
Used in Pharmaceutical Drug Development:
3-Chloroadamantane-1-carboxylic acid is employed as a key component in the creation of new pharmaceutical drugs, leveraging its unique framework to potentially develop novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 34859-74-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,5 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34859-74:
(7*3)+(6*4)+(5*8)+(4*5)+(3*9)+(2*7)+(1*4)=150
150 % 10 = 0
So 34859-74-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H15ClO2/c12-11-4-7-1-8(5-11)3-10(2-7,6-11)9(13)14/h7-8H,1-6H2,(H,13,14)/p-1/t7-,8-,10?,11?/m1/s1

34859-74-0 Well-known Company Product Price

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  • Alfa Aesar

  • (B20543)  3-Chloroadamantane-1-carboxylic acid, 97%   

  • 34859-74-0

  • 1g

  • 1077.0CNY

  • Detail
  • Alfa Aesar

  • (B20543)  3-Chloroadamantane-1-carboxylic acid, 97%   

  • 34859-74-0

  • 5g

  • 4306.0CNY

  • Detail

34859-74-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-CHLOROADAMANTANE-1-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 3-Chlor-adamantan-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:34859-74-0 SDS

34859-74-0Relevant academic research and scientific papers

Chlorination of Adamantane and Its Derivatives by Carbon Tetrachloride in the Presence of Manganese-, Vanadium-, and Molybdenum-containing Catalysts

Khusnutdinov,Shchadneva,Baiguzina,Lavrent'eva,Burangulova,Dzhemilev

, p. 126 - 133 (2007/10/03)

The feasibility of catalytic chlorination of adamantane and its derivatives by carbon tetrachloride in the presence of manganese-, vanadium-, and molybdenum-containing catalysts activated by nitrile ligands or alcohols was established. The optimum molar ratios of catalyst components and reactants and the optimum reaction conditions for selective syntheses of mono-, di-, and trichlorosubstituted adamantane derivatives with high yields were found.

PHOSPHORYLATED ADAMANTANES. XV. PHOSPHORYLATION OF ADAMANTANE WITH P(III) ACID CHLORIDES IN SULFURIC ACID

Yurchenko, R. I.,Peresypkina, L. P.,Miroshnichenko, V. V.,Yurchenko, A. G.

, p. 1072 - 1076 (2007/10/02)

A new method of introduction of a phosphoryl group into the nodal position of the adamantane nucleus was developed, in which sulfuric acid was used instead of aluminum halides to generate the adamantyl cation in reactions of Br-, OH-, and ONO2-substituted adamantanes and phosphonous and phosphorous chlorides. Relative rates of the hydride shift and skeletal isomerization were qualitatively estimated. Under comparable conditions the rate of the hydride shift in 2-adamantyl carbocation -> 1-adamantyl carbocation is substantially higher than that in the isomerization 1-ethyl-3-adamantyl carbocation -> 1,3-dimethyl-5-adamantyl carbocation.

ON THE MECHANISM OF LIQUID PHASE HALOGENATION OF ADAMANTANE DERIVATIVES

Yurchenko, A. G.,Kulik, N. I.,Kuchar, V. P.,Djakovskaja, V. M.,Baklan, V. F.

, p. 1399 - 1402 (2007/10/02)

The novel mechanistic representation of adamantane derivatives halogenation process is introduced.

SYNTHESIS AND CHEMICAL TRANSFORMATIONS OF ACETYLAMINO DERIVATIVES OF ADAMANTANE

Novikov, S. S.,Khardin, A. P.,Butenko, L. N.,Kulev, I. A.,Novakov, I. A.,et al.

, p. 1231 - 1232 (2007/10/02)

The synthesis of acetylamino derivatives of adamantane by the Ritter reaction in a mixture of sulfuric and nitric acids is described.Their hydrolysis in the presence of hydrochloric acid was investigated.

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