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14546-38-4

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14546-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14546-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,4 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14546-38:
(7*1)+(6*4)+(5*5)+(4*4)+(3*6)+(2*3)+(1*8)=104
104 % 10 = 4
So 14546-38-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO/c1-2-7-3-5-8(9-10)6-4-7/h3-6,9-10H,2H2,1H3

14546-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-ethylphenyl)hydroxylamine

1.2 Other means of identification

Product number -
Other names 4-ethyl-N-hydroxyaniline

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:14546-38-4 SDS

14546-38-4Upstream product

14546-38-4Relevant articles and documents

Expeditious and Efficient ortho-Selective Trifluoromethane-sulfonylation of Arylhydroxylamines

Liu, Yue,Bai, Songlin,Du, Yuanbo,Qi, Xiangbing,Gao, Hongyin

supporting information, (2021/12/27)

A metal- and oxidant-free, practical and efficient method for the synthesis of highly versatile and synthetically useful ortho-trifluoromethanesulfonylated anilines from arylhydroxylamines and trifluoromethanesulfinic chloride was developed. This rapid tr

Preparation, properties and infrared spectral studies of N-(p-ethylphenyl)thiobenzohydroxamic acid

Kakkar, Rita,Dua, Amita,Zaidi, Sheza

, p. 1362 - 1369 (2008/09/17)

The preparation of N-(p-ethylphenyl)thiobenzohydroxamic acid and its spectral properties are described in this paper. The preferred conformation of the acid is investigated by both infrared techniques and theoretical calculations at the DFT level. It is f

Method for producing 5-substituted-2-acylaminophenols, and 5-alkyl-2-acylaminophenol compound and N-acyl-N-(4-alkyl-phenyl)hydroxylamine compound

-

, (2008/06/13)

There is disclosed a method for producing 5-substituted-2-acylaminophenols of formula (I), comprising hydrolyzing to partially deacylate a compound of formula (V): ???in formulae (I) and (V), R1represents an aliphatic hydrocarbon group, an aliphatic hydrocarbon oxy group, an aryloxy group, an acylamino group, a disubstituted amino group, or a hydroxyl group; R2represents an acyl group; X1and X2each represent a hydrogen atom or a halogen atom; and R3represents an acyl group. According to the present invention, a method for synthesizing 2-acylaminophenols that uses inexpensive starting materials, has short steps, is environmentally friendly, is high in safety, and is low in cost, is provided.

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