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N-Boc-2-amino-3-bromothiophene, with the molecular formula C11H14BrNO2S, is a chemical compound derived from thiophene. It features a bromine atom and an amino group, with the Boc (tert-butoxycarbonyl) group acting as a protecting agent for the amino group. N-Boc-2-amino-3-bromothiophene is a crucial intermediate in organic synthesis, particularly for the development of pharmaceuticals and agrochemicals, due to its selective reactivity in chemical reactions.

85069-60-9

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85069-60-9 Usage

Uses

Used in Pharmaceutical Industry:
N-Boc-2-amino-3-bromothiophene is utilized as a key building block in the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the creation of novel drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, N-Boc-2-amino-3-bromothiophene serves as an essential intermediate for the development of new agrochemicals. Its properties and reactivity contribute to the design of innovative compounds with improved efficacy in agricultural applications.
Used in Organic Synthesis:
N-Boc-2-amino-3-bromothiophene is employed as a valuable intermediate in organic synthesis. Its selective reactivity, due to the Boc protecting group, enables the synthesis of complex organic molecules and biologically active compounds, advancing the fields of medicinal and agricultural chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 85069-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,6 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85069-60:
(7*8)+(6*5)+(5*0)+(4*6)+(3*9)+(2*6)+(1*0)=149
149 % 10 = 9
So 85069-60-9 is a valid CAS Registry Number.

85069-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(3-bromothiophen-2-yl)carbamate

1.2 Other means of identification

Product number -
Other names tert-Butyl (3-bromothiophen-2-yl)carbamate

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:85069-60-9 SDS

85069-60-9Downstream Products

85069-60-9Relevant academic research and scientific papers

Thienopyrrole acetic acids as antagonists of the CRTH2 receptor

Bonafoux, Dominique,Abibi, Ayome,Bettencourt, Brian,Burchat, Andrew,Ericsson, Anna,Harris, Christopher M.,Kebede, Tegest,Morytko, Michael,McPherson, Michael,Wallace, Grier,Wu, Xiaoyun

scheme or table, p. 1861 - 1864 (2011/05/05)

The bioisosteric replacement of the indole core of CRTH2 antagonists using thienopyrroles was investigated, resulting in potent antagonists with good selectivity over DP1. Early ADME/PK assessment of this chemotype demonstrated bioavailability in mice.

NOVEL THIENOPYRROLE COMPOUNDS

-

Page/Page column 44-45, (2011/07/06)

The invention provides a compound of Formula (I) pharmaceutically acceptable salts, pro-drugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variable are defined herein. The compounds of the invention are useful for treati

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