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3-iodo-2,4-dimethylaniline is an organic compound with the chemical formula C8H10IN. It is a derivative of aniline, where one hydrogen atom is replaced by an iodine atom at the 3rd position, and two methyl groups are attached to the 2nd and 4th positions of the benzene ring. 3-iodo-2,4-dimethylaniline is characterized by its molecular weight of 259.08 g/mol and a melting point of 54-56°C. It is a pale yellow solid and is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. 3-iodo-2,4-dimethylaniline is used in the synthesis of various pharmaceuticals, agrochemicals, and dyes due to its unique chemical structure and reactivity. It is also employed as a chemical intermediate in the production of other organic compounds.

4102-51-6

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4102-51-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4102-51-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,0 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4102-51:
(6*4)+(5*1)+(4*0)+(3*2)+(2*5)+(1*1)=46
46 % 10 = 6
So 4102-51-6 is a valid CAS Registry Number.

4102-51-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl α-hydroxy-α-(o-methoxyphenyl)acetate

1.2 Other means of identification

Product number -
Other names 2-Methoxy-mandelsaeure-aethylester

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:4102-51-6 SDS

4102-51-6Downstream Products

4102-51-6Relevant academic research and scientific papers

BETA-SUBSTITUTED BETA-AMINO ACIDS AND ANALOGS AS CHEMOTHERAPEUTIC AGENTS

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Paragraph 0536; 0635, (2015/09/22)

β-Substituted β-amino acids, β-substituted β-amino acid derivatives, and β-substituted β-amino acid analogs and (bio)isosteres and their use as chemotherapeutic agents are disclosed. The β-substituted β-amino acid derivatives and β-substituted β-amino acid analogs and (bio)isosteres are selective LAT1/4F2hc substrates and exhibit rapid uptake and retention in tumors expressing the LAT1/4F2hc transporter. Methods of synthesizing the β-substituted β-amino acid derivatives and β-substituted β-amino acid analogs and methods of using the compounds for treating cancer are also disclosed. The β-substituted β-amino acid derivatives and β-substituted β-amino acid analogs exhibit selective uptake in tumor cells expressing the LAT1/4F2hc transporter and accumulate in cancerous cells when administered to a subject in vivo. The β-substituted β-amino acid derivatives and β-substituted β-amino acid analogs and (bio)isosteres exhibit cytotoxicity toward several tumor types.

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