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22955-07-3

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22955-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22955-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,5 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22955-07:
(7*2)+(6*2)+(5*9)+(4*5)+(3*5)+(2*0)+(1*7)=113
113 % 10 = 3
So 22955-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H11NO4/c16-9-12-6-7-14(13(8-12)15(17)18)19-10-11-4-2-1-3-5-11/h1-9H,10H2

22955-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitro-4-phenylmethoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names OR0815

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:22955-07-3 SDS

22955-07-3Relevant articles and documents

Method for synthesizing aromatic aldehyde through iron catalyzed oxidation allyl aromatic compound

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Paragraph 0075-0077; 0150, (2019/06/27)

The invention discloses a method for synthesizing aromatic aldehyde through an iron catalyzed oxidation allyl aromatic compound. According to the specific method, under the promotion effect of hydrogen silane, with air or oxygen as the oxidant, the aromatic aldehyde compound is synthesized through the iron catalyzed oxidation allyl aromatic compound, the reaction temperature is 20-150 DEG C, and the time is 0.25-60 h. The method has the advantages that a catalyst source is wide, the price is low and the environment is protected; an oxidant source is wide, the price is low and no waste is generated; the reaction conditions are mild, selectivity is high and the yield is high; a substrate source is wide and stable; a substrate functional group is high in compatibility and a substrate is widein application range; complicated small molecules are compatible and can be well converted into aldehyde. The target product separation yield can reach up to 96% under the optimized reaction conditions.

A method for producing an optically active Alkylaminosulfonamide deriv. β-amino alcohol derivative and optically active

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Paragraph 0061; 0062; 0063, (2016/10/17)

PROBLEM TO BE SOLVED: To provide a method for producing an optically active alkylaminosulfonamide derivative useful in pharmaceutical applications etc., and an optically active β-aminoalcohol derivative. SOLUTION: The optically active alkylaminosulf

l , l , 3-TRI0X0-l , 2 , 5-THIADIAZ0LIDINES AND THEIR USE AS PTP-ASES INHIBITORS

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Page/Page column 55, (2010/11/27)

Compounds of the formula are inhibitors of protein tyrosine phosphatases (PTPases) and, thus, may be employed for the treatment of conditions mediated by PTPase activity. The compounds of the present invention may also be employed as inhibitors of other e

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