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59768-70-6

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59768-70-6 Usage

Chemical structure

Contains a bromo group attached to an adamantane group, with an acetic acid moiety

Derivative

1-adamantylacetic acid

Potential properties

Anti-inflammatory and immunomodulatory

Altered properties

The addition of the bromo group may alter its biological activity and pharmacological properties

Potential applications

Pharmaceutical research and drug development for the treatment of inflammatory and immune-related disorders

Further research needed

To fully understand its biological effects and potential therapeutic uses
It's worth noting that this is a brief summary of the main properties and specific content of 1-ADAMANTYL(BROMO)ACETIC ACID, and further research and studies are needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 59768-70-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,6 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59768-70:
(7*5)+(6*9)+(5*7)+(4*6)+(3*8)+(2*7)+(1*0)=186
186 % 10 = 6
So 59768-70-6 is a valid CAS Registry Number.

59768-70-6SDS

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-(1-adamantyl)-2-bromoacetic acid

1.2 Other means of identification

Product number -
Other names α-bromotricyclo[3.3.1.13,7]decane-1-acetic acid

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:59768-70-6 SDS

59768-70-6Relevant articles and documents

PROCESS FOR PREPARATION OF (IS, 3S, 5S)-2-[(2S)-2-AMIN0-2-(3-HYDROXY-l-ADAMANTYL) ACETYL]-2-AZABICYCLO [3.1.0] HEXANE-3-CARBONITRILE

-

Paragraph 0048, (2015/04/28)

Provided are novel processes for the preparation of Saxagliptin and novel intermediates employed in the process for preparing Saxagliptin.

Copper-catalyzed synthesis of azaspirocyclohexadienones from ∝-azido- N -arylamides under an oxygen atmosphere

Chiba, Shunsuke,Zhang, Line,Lee, Jian-Yuan

supporting information; experimental part, p. 7266 - 7267 (2010/08/05)

A copper-catalyzed reaction of ∝-azido-N-arylamides was found to proceed under an oxygen atmosphere to afford azaspirocyclohexadienones. The present transformation is carried out by a sequence of denitrogenative formation of iminyl copper species from ∝-azido-N-arylamides and their imino-cupration with an intramolecular benzene ring on the amido nitrogen followed by consecutive formation of C-O bonds. The preliminary investigation revealed that molecular oxygen is a prerequisite for achieving the present catalytic cyclization and that one of the oxygen atoms of O2 was found to be incorporated into the cyclohexadienone moiety.

α-AMINO ACIDS OF THE ADAMANTANE SERIES. III. DEAMINATION AS A METHOD FOR THE SYNTHESIS OF HOMOADAMANTANE DERIVATIVES

Krasutskii, P. A.,Semenova, I. G.,Safronova, E. E.,Novikova, M. I.,Yurchenko, A. G.

, p. 2106 - 2111 (2007/10/02)

The deamination of 1-adamantylglycine and its methyl-substituted analogs in acetic, trifluoroacetic, and sulfuric acids was investigated for the first time.The optimum conditions for the selective conversion of α-amino acids of the adamantane series into the β-hydroxy acids of homoadamantane are the conditions of solvolysis by the action of sodium nitrite in 70percent sulfuric acid.The synthetic transformations of 3-hydroxyhomoadamantane-4-carboxylic acid have opened up the way to the synthesis of new 3,4-disubstituted homoadamantanes.

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