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36383-33-2

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36383-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36383-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,8 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36383-33:
(7*3)+(6*6)+(5*3)+(4*8)+(3*3)+(2*3)+(1*3)=122
122 % 10 = 2
So 36383-33-2 is a valid CAS Registry Number.

36383-33-2SDS

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 (2-acetyloxy-4-nitrophenyl) acetate

1.2 Other means of identification

Product number -
Other names 4-Nitrobrenzcatechindiacetat

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:36383-33-2 SDS

36383-33-2Relevant articles and documents

Thiazolocatechol: Electron-Withdrawing Catechol Anchoring Group for Dye-Sensitized Solar Cells

Higashino, Tomohiro,Iiyama, Hitomi,Kurumisawa, Yuma,Imahori, Hiroshi

, p. 2689 - 2695 (2019)

Anchoring groups adopting a five-membered bidentate chelating are attractive to realize high power conversion efficiency (η) and long-term durability in dye-sensitized solar cells (DSSCs). In this regard, we chose catechol as an anchoring group that can a

Efficient synthesis of 5,6-dihydroxyindole dimers, key eumelanin building blocks, by a unified o-ethynylaniline-based strategy for the construction of 2-linked biindolyl scaffolds

Capelli, Luigia,Manini, Paola,Pezzella, Alessandro,Napolitano, Alessandra,D'Ischia, Marco

supporting information; experimental part, p. 7191 - 7194 (2009/12/09)

(Chemical Equation Presented) A unified convenient strategy for the synthesis of 5,6-dihydroxyindole-derived 2,7′-, 2,2′-, and 2,3′-biindolyls is reported, which is based on proper manipulation of key o-ethynylaniline precursors. By the same methodology 5

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