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253681-19-5

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253681-19-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 253681-19-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,6,8 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 253681-19:
(8*2)+(7*5)+(6*3)+(5*6)+(4*8)+(3*1)+(2*1)+(1*9)=145
145 % 10 = 5
So 253681-19-5 is a valid CAS Registry Number.

253681-19-5SDS

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 N-benzyl-2,6-dimethoxyaniline

1.2 Other means of identification

Product number -
Other names Benzyl-(2,6-dimethoxy-phenyl)-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:253681-19-5 SDS

253681-19-5Relevant articles and documents

Step-Economical Photoassisted Diversity-Oriented Synthesis: Sustaining Cascade Photoreactions in Oxalyl Anilides to Access Complex Polyheterocyclic Molecular Architectures

Kuznetsov, Dmitry M.,Kutateladze, Andrei G.

, p. 16584 - 16590 (2017/11/28)

Atom- and step-economy in photoassisted diversity-oriented synthesis (DOS) is achieved with a versatile oxalyl linker offering rapid access to complex alkaloid mimics in very few experimentally simple steps: (i) it allows for fast tethering of the photoac

Synthesis of novel orthoalkylaminophenol derivatives as potent neuroprotective agents in vitro.

Larget, Ronan,Lockhart, Brian,Pfeiffer, Bruno,Neudorffer, Anne,Fleury, Maurice-Bernard,Largeron, Martine

, p. 2929 - 2934 (2007/10/03)

A series of orthoalkylaminophenol derivatives was synthesized and tested in vitro with respect to their neuroprotective effect. Some of these compounds exhibited a potent antioxidant activity close to that of standard α-tocopherol.

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