Welcome to LookChem.com Sign In|Join Free

CAS

  • or
N-BOC-4-(2-BROMO-ACETYL)-ANILINE, also known as N-[(BUOXY)CARBONYL]-4-(2-BROMOACETYL)ANILINE, is a chemical compound with the molecular formula C12H14BrNO3 and a molecular weight of 304.15g/mol. It belongs to the category of Amino Acids, Peptides, and Proteins and their Derivatives. N-BOC-4-(2-BROMO-ACETYL)-ANILINE is prominently used in the field of organic chemistry, particularly in the synthesis of various pharmaceutical drugs and organic compounds. However, its physical properties and potential hazards require further research and adherence to safety protocols during handling.

885269-70-5 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 885269-70-5 Structure
  • Basic information

    1. Product Name: N-BOC-4-(2-BROMO-ACETYL)-ANILINE
    2. Synonyms: N-BOC-4-(2-BROMO-ACETYL)-ANILINE;[4-(Bromoacetyl)phenyl]carbamic acid tert-butyl ester;tert-Butyl (4-(2-broMoacetyl)phenyl)carbaMate;1-Piperazinepropanol, -alpha-,-alpha--dimethyl;[4-(2-Bromo-acetyl)-phenyl]-carbamic acid tert-butyl ester
    3. CAS NO:885269-70-5
    4. Molecular Formula: C13H16BrNO3
    5. Molecular Weight: 314.18
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 885269-70-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 357℃
    3. Flash Point: 169℃
    4. Appearance: /
    5. Density: 1.407
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.576
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: N-BOC-4-(2-BROMO-ACETYL)-ANILINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-BOC-4-(2-BROMO-ACETYL)-ANILINE(885269-70-5)
    12. EPA Substance Registry System: N-BOC-4-(2-BROMO-ACETYL)-ANILINE(885269-70-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 885269-70-5(Hazardous Substances Data)

885269-70-5 Usage

Uses

Used in Pharmaceutical Industry:
N-BOC-4-(2-BROMO-ACETYL)-ANILINE is used as a reagent for the synthesis of various pharmaceutical drugs and organic compounds. Its role in the synthesis process is crucial, as it contributes to the development of new and effective medications.
Used in Organic Chemistry Research:
In the field of organic chemistry, N-BOC-4-(2-BROMO-ACETYL)-ANILINE serves as a valuable compound for research purposes. It is utilized in the exploration of new chemical reactions and the development of innovative synthetic pathways, further expanding the understanding of organic chemistry and its applications.

Check Digit Verification of cas no

The CAS Registry Mumber 885269-70-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,6 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 885269-70:
(8*8)+(7*8)+(6*5)+(5*2)+(4*6)+(3*9)+(2*7)+(1*0)=225
225 % 10 = 5
So 885269-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H16BrNO3/c1-13(2,3)18-12(17)15-10-6-4-9(5-7-10)11(16)8-14/h4-7H,8H2,1-3H3,(H,15,17)

885269-70-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl (4-(2-bromoacetyl)phenyl)carbamate

1.2 Other means of identification

Product number -
Other names tert-butyl N-[4-(2-bromoacetyl)phenyl]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:885269-70-5 SDS

885269-70-5Relevant articles and documents

Alkoxy pyridone compound as well as preparation method and application thereof

-

, (2020/12/15)

The invention belongs to the field of medicinal chemistry, specifically, the invention relates to a series of inhibitors of factor XIa (FXIa for short) with a novel structure as well as a preparationmethod and an application thereof. The structure is shown as the following general formula (I). These compounds or stereoisomers, racemates, geometric isomers, tautomers, prodrugs, hydrates, solvatesor pharmaceutically acceptable salts and pharmaceutical compositions thereof can be used to treat or/and prevent related diseases mediated by factor XIa (FXIa for short).

INHIBITORS OF HISTONE DEACETYLASE

-

Paragraph 0275, (2016/04/26)

This invention provides compounds that are inhibitors of HDAC2. The compounds (e.g., compounds according to Formula (I), (II), (IIa), (III), (IV), (V), or (VI)) accordingly are useful for treating, alleviating, or preventing a condition in a subject such as a neurological disorder, memory or cognitive function disorder or impairment, extinction learning disorder, fungal disease or infection, inflammatory disease, hematological disease, or neoplastic disease, or for improving memory or treating, alleviating, or preventing memory loss or impairment.

Reversible photocontrol of peptide conformation with a rhodopsin-like photoswitch

Blanco-Lomas, Marina,Samanta, Subhas,Campos, Pedro J.,Woolley, G. Andrew,Sampedro, Diego

supporting information; scheme or table, p. 6960 - 6963 (2012/06/15)

Reversible photocontrol of biomolecules requires chromophores that can efficiently undergo large conformational changes upon exposure to wavelengths of light that are compatible with living systems. We designed a benzylidene-pyrroline chromophore that mimics the Schiff base of rhodopsin and can be used to introduce light-switchable intramolecular cross-links in peptides and proteins. This new class of photoswitch undergoes an ~10 A change in end-to-end distance upon isomerization and can be used to control the conformation of a target peptide efficiently and reversibly using, alternately, violet (400 nm) and blue (446 nm) light.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 885269-70-5