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ANTHRANILIC ACID, N-BOC-5-METHYL is a chemical compound derived from anthranilic acid, a white crystalline solid with a slight odor. It is characterized by the presence of the N-BOC-5-METHYL group, which serves as a protective group in organic synthesis to temporarily block reactive functional groups and prevent unwanted side reactions. ANTHRANILIC ACID, N-BOC-5-METHYL plays a significant role in organic chemistry and drug development, as it can be utilized to modify and protect specific functional groups during chemical reactions.

669713-60-4

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669713-60-4 Usage

Uses

Used in Pharmaceutical Industry:
ANTHRANILIC ACID, N-BOC-5-METHYL is used as an intermediate in the production of various drugs and dyes. Its protective N-BOC-5-METHYL group allows for the synthesis of complex molecules with controlled reactivity, facilitating the development of new pharmaceutical compounds.
Used in Organic Synthesis:
In the field of organic synthesis, ANTHRANILIC ACID, N-BOC-5-METHYL is employed as a protective agent for functional groups. The N-BOC-5-METHYL group temporarily blocks reactive sites, enabling chemists to carry out selective reactions and avoid unwanted side reactions. This selective protection is crucial for the synthesis of complex organic molecules and the development of novel chemical compounds.
Used in Dye Production:
ANTHRANILIC ACID, N-BOC-5-METHYL is also utilized in the production of dyes. Its unique chemical structure allows for the creation of dyes with specific properties, such as color, solubility, and stability. The protective group can be selectively removed during the synthesis process, enabling the production of dyes with desired characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 669713-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,9,7,1 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 669713-60:
(8*6)+(7*6)+(6*9)+(5*7)+(4*1)+(3*3)+(2*6)+(1*0)=204
204 % 10 = 4
So 669713-60-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO4/c1-8-5-6-10(9(7-8)11(15)16)14-12(17)18-13(2,3)4/h5-7H,1-4H3,(H,14,17)(H,15,16)

669713-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]benzoic acid

1.2 Other means of identification

Product number -
Other names 2-(tert-Butoxycarbonylamino)-5-methyl-benzoic acid

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:669713-60-4 SDS

669713-60-4Relevant academic research and scientific papers

A phosgene and peroxide-free one-pot tandem synthesis of isatoic anhydrides involving anthranilic acid, boc anhydride and 2-chloro-N-methyl pyridinium iodide

Verma, Chhaya,Sharma, Somesh,Pathak, Arunendra

supporting information, p. 6897 - 6899 (2019/04/10)

A phosgene and peroxide-free approach for the synthesis of isatoic anhydrides has been described. The synthesis involves the carbamate formation with boc anhydride followed by in situ cyclization to afford the isatoic anhydride. The importance of this synthetic strategy is in the ease of operation, scalability and preparation from readily available raw materials.

Synthesis of a quinolone library from ynones

Ward, Timothy R.,Turunen, Brandon J.,Haack, Torsten,Neuenswander, Benjamin,Shadrick, William,Georg, Gunda I.

experimental part, p. 6494 - 6497 (2011/02/24)

A library of 72 quinolones was synthesized from substituted anthranilic acids, using ynone intermediates. These masked β-dicarbonyl synthons allowed cyclization under milder conditions than previously reported quinolone syntheses.

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