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69825-49-6

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69825-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69825-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,2 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69825-49:
(7*6)+(6*9)+(5*8)+(4*2)+(3*5)+(2*4)+(1*9)=176
176 % 10 = 6
So 69825-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO2/c1-3-14-11(13)8-12-10-7-5-4-6-9(10)2/h4-7,12H,3,8H2,1-2H3

69825-49-6SDS

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 N-(2-methylphenyl)glycinate

1.2 Other means of identification

Product number -
Other names Benzothiazol-2-yl-o-tolyl-amine

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:69825-49-6 SDS

69825-49-6Relevant articles and documents

Perovskite as Recyclable Photocatalyst for Annulation Reaction of N-Sulfonyl Ketimines

Shi, Anzai,Sun, Kai,Chen, Xiaolan,Qu, Lingbo,Zhao, Yufen,Yu, Bing

supporting information, p. 299 - 303 (2022/01/04)

A sustainable and cost-effective manner for the photocatalytic annulation reaction of N-sulfonyl ketimines with N-arylglycines to synthesize imidazolidine-fused sulfamidates (31 examples) by employing CsPbBr3 as a heterogeneous photocatalyst has been developed. The catalyst CsPbBr3 can be simply recovered from the reaction mixture and reused at least five times without an obvious reduction in its photocatalytic reactivity, exhibiting a high catalyst economic feature.

Synthesis, antiproliferative, and antioxidant activities of substituted n-[(1,3,4-oxadiazol-2-yl) methyl] benzamines

Ahsan, Mohamed Jawed,Bakht, Mohamed Afroz,Balaraju, Tuniki,Bhandari, Lakshya,Geesi, Mohammed H.,Gorantla, Vasubabu,Hassan, Mohd. Zaheen,Hussain, Afzal,Jadav, Surender Singh,Khalilullah, Habibullah,Makkar, Shally,Rani, Sandhya,Riadi, Yassine,Singh, Rajan

, p. 145 - 154 (2020/02/29)

Background: Oxadiazole emerged as an important class of heterocyclic compound with diverse biological activities like anticancer, antitubercular, anticonvulsant, anti-tubulin, antimicrobial, anti-inflammatory, antioxidant etc. Objective: The objective of

Functionalization of N-arylglycine esters: Electrocatalytic access to C-C bonds mediated by n-Bu4NI

Luo, Mi-Hai,Jiang, Yang-Ye,Xu, Kun,Liu, Yong-Guo,Sun, Bao-Guo,Zeng, Cheng-Chu

supporting information, p. 499 - 505 (2018/03/21)

An efficient electrocatalytic functionalization of N-arylglycine esters is reported. The protocol proceeds in an undivided cell under constant current conditions employing the simple, cheap and readily available n-Bu4NI as the mediator. In addition, it is demonstrated that the mediated process is superior to the direct electrochemical functionalization.

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