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Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI), also known as tert-butyl 3-isoxazolylcarbamate, is a chemical compound with the molecular formula C7H11NO3. It is a versatile reagent in organic synthesis and pharmaceutical research, and also serves as a precursor in the synthesis of various pharmaceutical drugs. Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI) has potential applications in the agricultural industry, particularly in the development of new pesticides or herbicides. However, it is crucial to handle Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI) with care due to its potential adverse effects on human health and the environment if not properly managed and disposed of.

264600-97-7

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  • Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI)

    Cas No: 264600-97-7

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264600-97-7 Usage

Uses

Used in Organic Synthesis:
Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI) is used as a reagent in organic synthesis for the preparation of various chemical compounds. Its unique structure allows for versatile reactions and the formation of a wide range of products.
Used in Pharmaceutical Research:
In pharmaceutical research, Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI) is utilized as a precursor in the synthesis of various pharmaceutical drugs. Its properties make it a valuable component in the development of new medications.
Used in Agricultural Industry:
Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI) has potential applications in the agricultural industry, where it may be used in the development of new pesticides or herbicides. Its unique chemical structure could contribute to the creation of more effective and targeted agricultural chemicals.
Used in Environmental Management:
Proper handling, management, and disposal of Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI) are essential to minimize its potential adverse effects on human health and the environment. This includes the development of safe storage methods, waste disposal protocols, and guidelines for its use in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 264600-97-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,4,6,0 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 264600-97:
(8*2)+(7*6)+(6*4)+(5*6)+(4*0)+(3*0)+(2*9)+(1*7)=137
137 % 10 = 7
So 264600-97-7 is a valid CAS Registry Number.

264600-97-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(1,2-oxazol-3-yl)carbamate

1.2 Other means of identification

Product number -
Other names 3-N-Boc-aminoisoxazole

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:264600-97-7 SDS

264600-97-7Relevant articles and documents

Method for efficiently synthesizing N-3-isooxazole tert-butyl carbamate

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Paragraph 0030; 0034, (2019/03/08)

The invention discloses a method for efficiently synthesizing N-3-isooxazole tert-butyl carbamate. The synthetic route comprises the following steps: brominating a compound A to obtain a compound B, and reacting the compound B and a compound C to obtain a compound D; and reacting the compound D and di-tert-butyl dicarbonate ester, thereby obtaining the compound E. The reaction formula is as shownin the specification. The process method for synthesizing 3-aminoisoxazole is simple in process, cheap and readily available in raw materials, simple and convenient in operation and extremely suitablefor large-scale industrial production, and has very wide industrial application prospects and market value.

SUBSTITUTED ISOXAZOLINES AND THEIR USE AS ANTIBACTERIAL AGENTS

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, (2008/06/13)

Compounds of formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, wherein, for example, X is O, S or NH; HET is an optionally substituted C-linked 5-membered heteroaryl ring containing 2 to 4 heteroatoms independently selected from N, O and S; Q is selected from, for example, Q1 and Q2: R2 and R3 are independently hydrogen or fluoro; T is selected from a range of groups, for example, an N-linked (fully unsaturated) 5-membered heteroaryl ring system or a group of formula (TC5): wherein Rc is, for example, R13CO-, R13SO2- or R13CS-; wherein R13 is, for example, optionally substituted (1-10C)alkyl or R14C(O)O(1-6C)alkyl wherein R14 is optionally substituted (1-10C)alkyl; are useful as antibacterial agents; and processes for their manufacture and pharmaceutical compositions containing them are described

SUBSTITUTED ISOXAZOLES AND THE USE THEREOF AS ANTIBIOTICS

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Page 29, (2010/02/07)

Compounds of formula (I), wherein X is O, S, NH, OCO, NH-CO, NH-COO, NH-CO-NH, NH-CS or NH-CS-NH; R4 is H, (C1-C3)-alkyl optionally substituted by halogen, or a C-linked heterocyclic radical selected from several possibilities; R1 an

HETEROCYCLYLAMINOMETHYLOXAZOLIDINONES AS ANTIBACTERIALS

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Page/Page column 42, (2010/01/31)

Compounds of formula (I) or a pharmaceutically-acceptable salt, or an in-vivo hydrolysable ester thereof, wherein, for example,HET is an optionally substituted C-linked 5-membered heteroaryl ring containing 2 to 4 heteroatoms independently selected from N

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