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16200-53-6

16200-53-6

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16200-53-6 Usage

Chemical Properties

white crystalline powder and chunks or crystals

Check Digit Verification of cas no

The CAS Registry Mumber 16200-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,0 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16200-53:
(7*1)+(6*6)+(5*2)+(4*0)+(3*0)+(2*5)+(1*3)=66
66 % 10 = 6
So 16200-53-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O2/c11-9(12)10-4-6-1-7(5-10)3-8(10)2-6/h6-8H,1-5H2,(H,11,12)/p-1/t6-,7+,8?,10?

16200-53-6 Well-known Company Product Price

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  • Alfa Aesar

  • (A16683)  3-Noradamantanecarboxylic acid, 98%   

  • 16200-53-6

  • 0.25g

  • 328.0CNY

  • Detail

  • Alfa Aesar

  • (A16683)  3-Noradamantanecarboxylic acid, 98%   

  • 16200-53-6

  • 1g

  • 962.0CNY

  • Detail

  • Alfa Aesar

  • (A16683)  3-Noradamantanecarboxylic acid, 98%   

  • 16200-53-6

  • 5g

  • 4414.0CNY

  • Detail

16200-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-NORADAMANTANECARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 3-Carboxynoradamantane

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:16200-53-6 SDS

16200-53-6Relevant articles and documents

Compounds with urotropin structure. XLVII. A new synthesis of 1,2- and 2,6-disubstituted adamantanes

Stetter,Thomas,Meyer

, p. 863 - 867 (1970)

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Discovery of adamantane based highly potent HDAC inhibitors

Gopalan, Balasubramanian,Ponpandian, Thanasekaran,Kachhadia, Virendra,Bharathimohan, Kuppusamy,Vignesh, Radhakrishnan,Sivasudar, Velaiah,Narayanan, Shridhar,Mandar, Bhonde,Praveen, Rajendran,Saranya, Nithyanandan,Rajagopal, Sriram,Rajagopal, Sridharan

, p. 2532 - 2537 (2013/06/27)

Herein, we report the development of highly potent HDAC inhibitors for the treatment of cancer. A series of adamantane and nor-adamantane based HDAC inhibitors were designed, synthesized and screened for the inhibitory activity of HDAC. A number of compounds exhibited GI50 of 10-100 nM in human HCT116, NCI-H460 and U251 cancer cells, in vitro. Compound 32 displays efficacy in human tumour animal xenograft model.

SYNTHESIS OF 3-NORADAMANTAMINE

Jawdosiuk, Mikolaj,Kovacic, Peter

, p. 53 - 62 (2007/10/02)

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