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5814-40-4

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5814-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5814-40-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,1 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5814-40:
(6*5)+(5*8)+(4*1)+(3*4)+(2*4)+(1*0)=94
94 % 10 = 4
So 5814-40-4 is a valid CAS Registry Number.

5814-40-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(2-aminoanilino)benzoate

1.2 Other means of identification

Product number -
Other names -

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:5814-40-4 SDS

5814-40-4Relevant articles and documents

Tricyclic heterocycles display diverse sensitivity to the A147T TSPO polymorphism

Sokias, Renee,Werry, Eryn L.,Alison Cheng, Hei Wun,Lloyd, James H.,Sohler, Greta,Danon, Jonathan J.,Montgomery, Andrew P.,Du, Jonathan J.,Gao, Quanqing,Hibbs, David E.,Ittner, Lars M.,Reekie, Tristan A.,Kassiou, Michael

, (2020/09/17)

The 18 kDa translocator protein (TSPO) is a target for the development of imaging agents to detect neuroinflammation. The clinical utility of second-generation TSPO ligands has been hindered by the presence of a polymorphism, rs6971, which causes a non-co

Dibenzo-fused seven-membered nitrogen heterocycles by a tandem reduction-lactamization reaction

Bunce, Richard A.,Schammerhorn, James E.

, p. 1031 - 1035 (2007/10/03)

Efficient syntheses of dibenz[b,f][1,4]oxazepin-11(10H)-one, 5,10-dihydro-11H-dibenzo[b,e][1,4]-diazepin-11-one and 5,11-dihydro-6H-dibenz[b, e]azepin-6-one are described using a tandem reduction-lactamization sequence. Precursors for these ring systems are available in 1-3 steps using nucleophilic aromatic substitution and Ullmann coupling methodology. Direct reduction-lactamization of these compounds using iron powder in acetic acid at 115° affords the target heterocycles in ≥90% yield.

Metal Template Reactions. XVII. The Attempted Dimerization of Amino Carbonyl Compounds Containing a Supporting Donor Atom

Black, David St. C.,Rothnie, Neil E.

, p. 1149 - 1157 (2007/10/02)

Attempts to effect metal template condensative dimerizations of the amino aldehydes (4), (11) and (12) and the amino ketone (24) have been unsuccessful.Oxidation of the alcohol (9) did not allow isolation of the aldehyde (4).The alcohol (17) underwent oxi

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