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42091-29-2

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42091-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42091-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,9 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 42091-29:
(7*4)+(6*2)+(5*0)+(4*9)+(3*1)+(2*2)+(1*9)=92
92 % 10 = 2
So 42091-29-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H15NO3/c1-2-20-16(19)13-10-6-7-11-14(13)17-15(18)12-8-4-3-5-9-12/h3-11H,2H2,1H3,(H,17,18)

42091-29-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-benzamidobenzoate

1.2 Other means of identification

Product number -
Other names N-Benzoylanthranilsaeureaethylester

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:42091-29-2 SDS

42091-29-2Relevant articles and documents

Single-pot tandem oxidative/C-H modification amidation process using ultrasmall PdNP-encapsulated porous organosilica nanotubes

Gholipour, Behnam,Liu, Xiao,Rostamnia, Sadegh,Zonouzi, Afsaneh

, p. 4276 - 4287 (2022/02/16)

Herein, we studied a single-pot method with a dual catalysis process towards the conversion of primary aromatic alcohols to amides using ultrasmall PdNPs of controlled uniform size (1.8 nm) inside hybrid mesoporous organosilica nanotubes (MO-NTs). The cat

Selective Oxidative Decarbonylative Cleavage of Unstrained C(sp3)-C(sp2) Bond: Synthesis of Substituted Benzoxazinones

Verma, Ajay,Kumar, Sangit

, p. 4388 - 4391 (2016/10/11)

A transition metal (TM)-free practical synthesis of biologically relevant benzoxazinones has been established via a selective oxidative decarbonylative cleavage of an unstrained C(sp3)-C(sp2) bond employing iodine, sodium bicarbonate, and tbutyl hydroperoxide in DMSO at 95 °C. Control experiments and Density Functional Theory (DFT) calculations suggest that the reaction involves a [1,5]H shift and extrusion of CO gas as the key steps. The extrusion of CO has also been established using PMA-PdCl2.

N-Benzoyl-N-methylsulfonylanthranilates: Unexpected cyclization reaction to 4-alkoxy-2,1-benzothiazines

Manfroni, Giuseppe,Meschini, Francesco,Costantino, Ferdinando,Tabarrini, Oriana,Cecchettia, Violetta

, p. 165 - 176 (2011/08/07)

The synthesis of 4-alkoxy-1H-2,1-benzothiazine 2,2-dioxide derivatives was achieved through an unexpected base-mediated cyclization of N-benzoyl-N- methylsulfonylanthranilates. A reaction mechanism involving the sulfene species has been postulated. The ob

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