Welcome to LookChem.com Sign In|Join Free
  • or
Benzenamine, 3-bromo-2,5-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115929-62-9

Post Buying Request

115929-62-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

115929-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115929-62-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,9,2 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115929-62:
(8*1)+(7*1)+(6*5)+(5*9)+(4*2)+(3*9)+(2*6)+(1*2)=139
139 % 10 = 9
So 115929-62-9 is a valid CAS Registry Number.

115929-62-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-2,5-dimethoxyaniline

1.2 Other means of identification

Product number -
Other names 3-bromo-2,5-dimethoxy-aniline

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:115929-62-9 SDS

115929-62-9Downstream Products

115929-62-9Relevant academic research and scientific papers

A formal synthesis of lavendamycin methyl ester, nitramarine, and their analogues: A povarov approach

Ramesh, Subburethinam,Nagarajan, Rajagopal

, p. 545 - 558 (2013/03/14)

A convergent formal synthesis of lavendamycin methyl ester and synthesis of its analogues have been delineated through the Povarov approach. This protocol is also applied to the formal synthesis of nitramarine (3) in good yield.

An efficient method for aryl nitro reduction and cleavage of azo compounds using iron powder/calcium chloride

Chandrappa,Vinaya,Ramakrishnappa,Rangappa

experimental part, p. 3019 - 3022 (2011/03/17)

A novel, efficient Fe/CaCl2 system is revealed for the reduction of nitroarenes and reductive cleavage of azo compounds by catalytic transfer hydrogenation (CTH). The selective reduction of nitro compounds in the presence of sensitive functional groups including halides, carbonyl, hydroxyl, aldehyde, methyl, methoxy, acetyl, nitrile, and ester substituents with an excellent yields is reported. The simple experimental procedure and easy purification make the protocol advantageous

Aryl nitro reduction with iron powder or stannous chloride under ultrasonic irradiation

Gamble, Allan B.,Garner, James,Gordon, Christopher P.,O'Conner, Sean M. J.,Keller, Paul A.

, p. 2777 - 2786 (2008/02/12)

The selective reduction of aryl nitro compounds in the presence of sensitive functionalities, including halide, carbonyl, nitrile, and ester substituents, under ultrasonic irradiation at 35 kHz is reported in yields of 39-98%. Iron powder proved superior to stannous chloride with high tolerance of sensitive functional groups and high yields of the desired aryl amines in relatively short reaction times. Simple experimental procedure and purification also make the iron reduction of aryl nitro compounds advantageous over other methods of reduction. Copyright Taylor & Francis Group, LLC.

Total synthesis of herbimycin A

Canova, Sophie,Bellosta, Veronique,Bigot, Antony,Mailliet, Patrick,Mignani, Serge,Cossy, Janine

, p. 145 - 148 (2007/10/03)

(Chemical Equation Presented) Hsp90 has recently emerged as a promising biological target for treatment of cancer. Herbimycin A and other members of the benzoquinoid ansamycin class of natural products are known to inhibit Hsp90 activity. The total synthesis of herbimycin A was achieved from the commercially available Roche ester 1 by using allylmetals to control the stereogenic centers at C6, C7, C10, C11, and C12 and a ring-closing metathesis to control the (Z)-double bond of the (E,Z)-dienic moiety.

Synthesis of antitumor ansamycins. 2. A formal synthesis of (±)-macbecin I

Coutts,Kallmerten

, p. 4305 - 4308 (2007/10/02)

Convergent synthesis of (±)-2, a key intermediate in the Merck synthesis of macbecin I (1), incorporates the chelation-mediated coupling of a lithiated aryl subunit and the γ-hydroxy aldehyde equivalent 8 to establish a critical connective element of the

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 115929-62-9