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O-[(2-Chloro-6-fluorophenyl)methyl]hydroxylamine hydrochloride, also known as N-(2-Chloro-6-fluorobenzyl)hydroxylamine hydrochloride, is a chemical compound characterized by a hydroxylamine group attached to a benzyl group, featuring chlorine and fluorine atom substituents. O-[(2-Chloro-6-fluorophenyl)methyl]hydroxylamine hydrochloride is utilized in organic chemistry as a reagent for the preparation of various compounds and serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its potential applications in medicinal chemistry are notable, particularly as an anti-tumor agent, due to its ability to inhibit tumor growth and induce apoptosis in cancer cells. Careful handling is essential due to its potential hazards if not used properly.

93081-15-3

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93081-15-3 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
O-[(2-Chloro-6-fluorophenyl)methyl]hydroxylamine hydrochloride is used as a reagent for the preparation of various compounds in the pharmaceutical and agrochemical industries, facilitating the synthesis of a range of products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, O-[(2-Chloro-6-fluorophenyl)methyl]hydroxylamine hydrochloride is used as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs.
Used in Antitumor Applications:
O-[(2-Chloro-6-fluorophenyl)methyl]hydroxylamine hydrochloride is used as an anti-tumor agent for its potential to inhibit tumor growth and induce apoptosis in cancer cells, offering a promising avenue for cancer treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 93081-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,0,8 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93081-15:
(7*9)+(6*3)+(5*0)+(4*8)+(3*1)+(2*1)+(1*5)=123
123 % 10 = 3
So 93081-15-3 is a valid CAS Registry Number.

93081-15-3SDS

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 O-(2-Chloro-6-fluorobenzyl)hydroxylamine hydrochloride

1.2 Other means of identification

Product number -
Other names O-[(2-chloro-6-fluorophenyl)methyl]hydroxylamine,hydrochloride

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:93081-15-3 SDS

93081-15-3Upstream product

93081-15-3Relevant academic research and scientific papers

Synthesis and fungicidal activity of macrolactams and macrolactones with an oxime ether side chain

Huang, Jia-Xing,Jia, Yue-Mei,Liang, Xiao-Mei,Zhu, Wei-Juan,Zhang, Jian-Jun,Dong, Yan-Hong,Yuan, Hui-Zu,Qi, Shu-Hua,Wu, Jin-Ping,Chen, Fu-Heng,Wang, Dao-Quan

experimental part, p. 10857 - 10863 (2009/11/30)

Three series of novel macrolactams and macrolactones - 12-alkoxyimino- tetradecanlactam, 12-alkoxyiminopentadecanlactam, and 12-alkoxyiminodecanlactone derivatives (7A, 7B, and 7C) - were synthesized from corresponding 12-oxomacrolactams and 12-oxomacrolactone. Their structures were confirmed by 1H NMR and elemental analysis. The Z and E isomers of 7A and 7B were separated, and their configurations were determined by 1H NMR. These compounds showed fair to excellent fungicidal activities against Rhizoctonia solani Kuehn. It is interesting that the Z and E isomers of most of the compounds have quite different fungicidal activities. The fact that the compounds have a gradual increase of fungicidal activity in the order of 7A, 7C, and 7B indicated that the macrocyclic derivatives with a hydrogen-bonding acceptor (=N-O-) and a hydrogen-bonding donor (-CONH-) on the ring, and a three methylenes distance (CH2CH2CH2) between these two functional groups, exhibited the best fungicidal activity. The bioassay also showed that 7B not only has good fungicidal activity but also may have a broad spectrum of fungicidal activities.

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