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Phenol, 3-amino-, benzoate (ester), also known as 3-aminophenol benzoate, is a chemical compound with the molecular formula C13H11NO3. It is formed by the esterification of 3-aminophenol with benzoic acid, resulting in an ester linkage between the two molecules. Phenol, 3-amino-, benzoate (ester) is an organic derivative of phenol, characterized by the presence of an amino group (-NH2) at the 3-position on the phenol ring. 3-aminophenol benzoate is a white crystalline solid with a melting point of approximately 150°C. It is used in various applications, including the synthesis of dyes, pharmaceuticals, and other organic compounds. Due to its reactivity, it is important to handle Phenol, 3-amino-, benzoate (ester) with care, as it may cause irritation or other adverse effects upon contact with skin, eyes, or ingestion.

720-97-8

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720-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 720-97-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 720-97:
(5*7)+(4*2)+(3*0)+(2*9)+(1*7)=68
68 % 10 = 8
So 720-97-8 is a valid CAS Registry Number.

720-97-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-aminophenyl benzoate

1.2 Other means of identification

Product number -
Other names benzoic acid-(3-amino-phenyl ester)

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:720-97-8 SDS

720-97-8Relevant academic research and scientific papers

HIGHLY CHEMOSELECTIVE REACTIONS IN PRESENCE OF AROMATIC AMINO GROUPS

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Page/Page column 33; 37, (2017/11/06)

: The invention discloses a novel process for highly chemoselective reactions of substituted anilines without any detectable reaction at aromatic amino group. The invention also relates to a novel process for preparation of neostigmine methylsulphate via chemoselective reaction of 3-amionphenol and aryl dimethylcarbamates.

μ-Oxo-Dinuclear-Iron(III)-Catalyzed O-Selective Acylation of Aliphatic and Aromatic Amino Alcohols and Transesterification of Tertiary Alcohols

Horikawa, Rikiya,Fujimoto, Chika,Yazaki, Ryo,Ohshima, Takashi

, p. 12278 - 12281 (2016/08/24)

A highly chemoselective and reactive μ-oxo-dinuclear iron(III) salen catalyst for transesterification was developed. The developed iron complex catalyzed acylation of aliphatic amino alcohols with nearly perfect O-selectivity, even when using activated esters, for which chemoselectivity is more difficult to control. In addition, O-selective transesterification of aromatic amino alcohols was achieved for the first time. The high activity of the iron complex enabled the use of sterically congested tertiary alcohols, including unprecedented tert-butanol.

SILYL POLYMERIC BENZOIC ACID ESTER COMPOUNDS, USES, AND COMPOSITIONS THEREOF

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, (2011/05/05)

The present invention relates to organosilicon polymers containing benzoic acid esters in form of particles, process for their preparation, cosmetic or dermatological composition comprising them, as well as their use for protecting a human or animal livin

Silyl polymeric benzoic acid ester compounds, uses, and compositions thereof

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, (2011/05/05)

The present invention relates to organosilicon polymers containing benzoic acid esters in form of particles, process for their preparation, cosmetic or dermatological composition comprising them, as well as their use for protecting a human or animal livin

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