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ANTHRANILIC ACID, N-BOC-4-CHLORO, also known as tert-butyl 4-chloro-2-aminobenzoate, is a chemical compound with the chemical formula C11H12ClNO4. It is primarily used in the pharmaceutical industry as a reagent or an intermediate compound in drug manufacturing processes. This light yellow crystalline powder is essential in chemical synthesis, particularly in the production of molecules with bioactive properties.

136290-47-6

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136290-47-6 Usage

Uses

Used in Pharmaceutical Industry:
ANTHRANILIC ACID, N-BOC-4-CHLORO is used as a reagent for the synthesis of various pharmaceutical compounds. Its role in the production of bioactive molecules makes it a valuable component in drug development.
Used in Chemical Synthesis:
ANTHRANILIC ACID, N-BOC-4-CHLORO is used as an intermediate compound in the synthesis of complex molecules with potential applications in various fields, including medicine and biotechnology. Its versatility in chemical reactions contributes to the creation of new and innovative compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 136290-47-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,9 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 136290-47:
(8*1)+(7*3)+(6*6)+(5*2)+(4*9)+(3*0)+(2*4)+(1*7)=126
126 % 10 = 6
So 136290-47-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H14ClNO4/c1-12(2,3)18-11(17)14-9-6-7(13)4-5-8(9)10(15)16/h4-6H,1-3H3,(H,14,17)(H,15,16)

136290-47-6SDS

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 4-chloro-2-[(2-methylpropan-2-yl)oxycarbonylamino]benzoic acid

1.2 Other means of identification

Product number -
Other names 2-((tert-Butoxycarbonyl)amino)-4-chlorobenzoic 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:136290-47-6 SDS

136290-47-6Relevant academic research and scientific papers

SUBSTITUTED 1-ALKYLCINNOLIN-4(1H)-ONE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC APPLICATION OF SAME

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Page/Page column 8, (2012/06/01)

The subject of the present invention is compounds corresponding to the formula (I) in which: X represents a divalent (C2-C5)alkylene radical which is unsubstituted or substituted one or more times by an Alk group; R1 represents a phenyl, a naphthyl, a pyridyl, a 1-benzothienyl or a 1,3-benzodioxolyl; R2 represents a hydrogen atom, a halogen atom, an Alk group, an OAlk group or else a group chosen from —S-Alk, —SO-Alk, —SO2-Alk, —CO—N(R4)-Alk, —N(R4)SO2-Alk, —N(R4)CO-Alk, —N(R4)SO2—N(Alk)2; R3 represents a hydrogen atom, a halogen atom, an Alk group or an OAlk group; R4 represents a hydrogen atom or a (C1-C4)alkyl; Alk represents an unsubstituted or substituted (C1-C4)alkyl. Preparation process and therapeutic application.

SUBSTITUTED 1-BENZYL-CINNOLIN-4(1H)-ONE DERIVATIVES, PREPARATION THEREOF, AND THERAPEUTIC USE THEREOF

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Page/Page column 7, (2011/06/26)

The present invention is related to novel substituted 1-benzylcinnolin-4(1H)-one derivatives having affinity for cannabinoid CB2 receptors, their preparation and their therapeutic application.

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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