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3-Methoxyphenyl dimethylsulfamate is an organic compound with the chemical formula C9H13NO3S. It is a derivative of anisole, featuring a methoxy group (-OCH3) attached to the phenyl ring, and a dimethylsulfamoyl group (-S(=O)(=O)N(CH3)2) as a substituent. 3-methoxyphenyl dimethylsulfamate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a precursor in the production of sulfonamide antibiotics. The presence of the methoxy group can influence the electronic properties and reactivity of the molecule, making it a valuable intermediate in organic synthesis.

1138-66-5

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1138-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1138-66-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1138-66:
(6*1)+(5*1)+(4*3)+(3*8)+(2*6)+(1*6)=65
65 % 10 = 5
So 1138-66-5 is a valid CAS Registry Number.

1138-66-5Relevant academic research and scientific papers

N -Arylation of (hetero)arylamines using aryl sulfamates and carbamates via C-O bond activation enabled by a reusable and durable nickel(0) catalyst

Dindarloo Inaloo, Iman,Majnooni, Sahar,Eslahi, Hassan,Esmaeilpour, Mohsen

, p. 13266 - 13278 (2020/10/07)

An effective and general aryl amination protocol has been developed using a magnetically recoverable Ni(0) based nanocatalyst. This new stable catalyst was prepared on Fe3O4@SiO2 modified by EDTA and investigated by FT-IR, EDX, TEM, XRD, DLS, FE-SEM, XPS, NMR, TGA, VSM, ICP and elemental analysis techniques. The reaction proceeded via carbon-oxygen bond cleavage of (hetero)aryl carbamates and sulfamates under simple and mild conditions without the use of any external ligands. This method demonstrated functional group tolerance in the N-arylation of various nitrogen-containing compounds as well as aliphatic amines, anilines, pyrroles, pyrazoles, imidazoles, indoles, and indazoles with good to excellent yields. Furthermore, the catalyst could be easily recovered by using an external magnetic field and directly reused at least six times without notable reduction in its activity. This journal is

Ni(COD)2/PCy3 catalyzed cross-coupling of aryl and heteroaryl neopentylglycolboronates with aryl and heteroaryl mesylates and sulfamates in THF at room temperature

Leowanawat, Pawaret,Zhang, Na,Resmerita, Ana-Maria,Rosen, Brad M.,Percec, Virgil

experimental part, p. 9946 - 9955 (2012/01/15)

Reaction conditions for the Ni(COD)2/PCy3 catalyzed cross-coupling of aryl neopentylglycolboronates with aryl mesylates were developed. By using optimized reaction conditions, Ni(COD)2/PCy 3 was shown to be a versatile catalyst for the cross-coupling of a diversity of aryl neopentylglycolboronates with aryl and heteroaryl mesylates and sulfamates containing both electron-donating and electron-withdrawing substituents in their para, ortho, and meta positions in THF at room temperature. This Ni-catalyzed cross-coupling of aryl neopentylglycolboronates is also effective for the synthesis of heterobiaryls and biaryls containing electrophilic functionalities sensitive to organolithium and organomagnesium derivatives. In combination with the recently developed Nicatalyzed neopentylglycolborylation, all Ni-catalyzed routes to functional biaryls and heterobiaryls are now easily accessible (Figure presented).

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