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4055-69-0

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4055-69-0 Usage

Synthesis Reference(s)

Synthetic Communications, 16, p. 645, 1986 DOI: 10.1080/00397918608057734

Check Digit Verification of cas no

The CAS Registry Mumber 4055-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,5 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4055-69:
(6*4)+(5*0)+(4*5)+(3*5)+(2*6)+(1*9)=80
80 % 10 = 0
So 4055-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O4/c1-12-6-3-2-5(4-9)7(10)8(6)11/h2-4,10-11H,1H3

4055-69-0SDS

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 2,3-DIHYDROXY-4-METHOXYBENZALDEHYDE

1.2 Other means of identification

Product number -
Other names Benzaldehyde,2,3-dihydroxy-4-methoxy

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:4055-69-0 SDS

4055-69-0Relevant articles and documents

Synthesis and biological evaluation of 10-benzyloxy-Narciclasine

Ticli, Vincenzo,Zhao, Zhenze,Du, Liqin,Kornienko, Alexander,Hudlicky, Tomas

, (2021/11/08)

A chemoenzymatic convergent synthesis of 10-benzyloxy narciclasine from bromobenzene was accomplished in 16 steps. The key transformations included toluene dioxygenase-mediated hydroxylation, nitroso Diels-Alder reaction and intramolecular Heck cyclization. The unnatural derivative of narciclasine was subjected to biological evaluation and its activity was compared to other C-10 and C-7 compounds prepared previously.

Bioreductively Activatable Prodrug Conjugates of Combretastatin A-1 and Combretastatin A-4 as Anticancer Agents Targeted toward Tumor-Associated Hypoxia

Chaplin, David J.,Davis, Peter,Devkota, Laxman,Gerberich, Jeni L.,Hamel, Ernest,Kuch, Bunnarack,Macdonough, Matthew T.,Mason, Ralph P.,Mondal, Deboprosad,Pinney, Kevin G.,Ramirez, Alejandro J.,Shi, Zhe,Strecker, Tracy E.,Trawick, Mary Lynn,Wang, Yifan,Winn, Blake A.

, (2020/03/30)

The natural products combretastatin A-1 (CA1) and combretastatin A-4 (CA4) function as potent inhibitors of tubulin polymerization and as selective vascular disrupting agents (VDAs) in tumors. Bioreductively activatable prodrug conjugates (BAPCs) can enha

3-substituted coumarin derivatives and their use

-

Paragraph 0182; 0183; 0184, (2016/10/08)

The invention provides a 3-substituted coumarin derivative, and pharmaceutically acceptable salts, solvates, hydrates or crystal forms thereof. The above compound has a high calcium flow activity and a very good selectivity on a human derived cannabinoid receptor CB2, and is a specific agonist or inverse agonist of the cannabinoid receptor CB2. The compound is an active ligand of a novel cannabinoid II receptor CB2, and compounds of the above kind and pharmaceutically acceptable salts, solvates, hydrates or crystal forms thereof have high calcium flow activities and a very good selectivity on the human derived cannabinoid receptor CB2. The compound is the specific agonist or inverse agonist of the cannabinoid receptor CB2, and can be applied to the preparation of medicines for treating, preventing and inhibiting CB2 receptor mediated diseases. The structure of the derivative is represented by a general formula A shown in the specification.

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