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2592-05-4

2592-05-4

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2592-05-4 Usage

Chemical Properties

Red Solid

Uses

Intermediate in the preparation of Brassinin.

Check Digit Verification of cas no

The CAS Registry Mumber 2592-05-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2592-05:
(6*2)+(5*5)+(4*9)+(3*2)+(2*0)+(1*5)=84
84 % 10 = 4
So 2592-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O/c12-11-6-7-5-10-9-4-2-1-3-8(7)9/h1-6,11-12H/b7-6+

2592-05-4 Well-known Company Product Price

  • Brand
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  • Alfa Aesar

  • (H54754)  Indole-3-carboxaldoxime, 97%   

  • 2592-05-4

  • 250mg

  • 392.0CNY

  • Detail

  • Alfa Aesar

  • (H54754)  Indole-3-carboxaldoxime, 97%   

  • 2592-05-4

  • 1g

  • 1176.0CNY

  • Detail

  • Alfa Aesar

  • (H54754)  Indole-3-carboxaldoxime, 97%   

  • 2592-05-4

  • 5g

  • 4704.0CNY

  • Detail

2592-05-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(Z)-indol-3-ylidenemethyl]hydroxylamine

1.2 Other means of identification

Product number -
Other names Indole-3-aldehyde oxime

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:2592-05-4 SDS

2592-05-4Upstream product

2592-05-4Relevant articles and documents

Chemical structures of novel maillard reaction products under hyperglycemic conditions

Imahori, Daisuke,Matsumoto, Takahiro,Kojima, Naoto,Hasei, Tomohiro,Sumii, Megumi,Sumida, Taishi,Yamashita, Masayuki,Watanabe, Tetsushi

, p. 363 - 367 (2018/04/09)

Two novel and two known compounds, 4-quinolylaldoxime and indole-3-aldehyde, were isolated from a reaction mixture consisting of D-glucose and L-tryptophan at physiological temperature and pH. The chemical structures of the two novel compounds were elucidated by spectroscopic analysis such as X-ray crystallography. One of the novel compound and the indole-3-aldehyde showed mutagenicity toward Salmonella typhimurium YG1024 with S9 mix. Furthermore, 4-quinolylaldoxime was detected from streptozotocin-induced diabetic rat plasma by LC-MS/MS analysis; however, the isolated compounds were not detected in rat diet extracts. To our knowledge, this is the first report in which 4-quinolylaldoxime was detected in rat plasma. These results suggest that amino-carbonyl reaction products may be formed in diabetic condition and induce genetic damage.

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