1208070-80-7

Basic information

• Product Name: 2-bromo-4-methylphenylcyanamide
• Synonyms: 2-bromo-4-methylphenylcyanamide
• CAS NO: 1208070-80-7
• Molecular Weight: 211.061
• Mol File: 1208070-80-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-bromo-4-methylphenylcyanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-4-methylphenylcyanamide(1208070-80-7)
• EPA Substance Registry System: 2-bromo-4-methylphenylcyanamide(1208070-80-7)

Safety Data

• Hazardous Substances Data: 1208070-80-7(Hazardous Substances Data)

Upstream product

• 10532-64-6 N-(4-methylphenyl)cyanamide 
• 19241-39-5 (2-bromo-4-methylphenyl)isothiocyanate 
• 58655-25-7 C₆H₁₅N*C₈H₈BrNS₂ 
• 1334247-59-4 C₈H₉BrN₂Se 
• 66644-79-9 2-Bromo-4-methylphenylthiourea 

Relevant articles and documents

Efficient Pd(ii)-catalyzed regioselectiveortho-halogenation of arylcyanamides

Regioselectiveortho-halogenation of arylcyanamides using a Pd(ii) catalyst has been established under mild reaction conditions. Either electron-donating or electron-withdrawing groups readily carried out the reaction and produced final products in moderate to good yields. Based on the experimental work, we have confirmed that this method does not undergo a free radical mechanism. Furthermore, we have also attempted this method for practical utility purposes.

Copper-catalyzed domino one-pot synthesis of 2-(arylselanyl)arylcyanamides

Domino C-Se cross-coupling of 2-(iodoaryl)selenoureas with aryl iodides has been accomplished in the presence of a copper(I)-1,1-phenanthroline complex at moderate temperature. The reactions involve intra- and intermolecular C-Se cross-coupling to give th

A one-pot preparation of cyanamide from dithiocarbamate using molecular iodine

An efficient one-pot method for the synthesis of cyanamides from dithiocarbamate salts via a double desulfurization strategy using molecular iodine is disclosed. Dithiocarbamates, by the action of iodine yield isothiocyanates in situ, which on treatment with aqueous NH3 give thioureas. The thioureas so generated undergo further oxidative desulfurization with I2 giving corresponding cyanamides in good yields. Environmental benignity, cost effectiveness and high yields are the important attributes of this one pot procedure. The Royal Society of Chemistry 2009.