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Carbamic acid, (2-bromocyclohexyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119027-93-9

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119027-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119027-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,2 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 119027-93:
(8*1)+(7*1)+(6*9)+(5*0)+(4*2)+(3*7)+(2*9)+(1*3)=119
119 % 10 = 9
So 119027-93-9 is a valid CAS Registry Number.

119027-93-9Downstream Products

119027-93-9Relevant academic research and scientific papers

CHROMIUM(II) PROMOTED ADDITION OF N-CHLOROCARBAMATES TO ALKENES

Gerber, J. P.,Goosen, A.,McCleland, C. W.

, p. 3037 - 3051 (2007/10/02)

Ethyl N-chloro-N-methylcarbamate has been shown to produce adducts with some alkenes.The role of the chromium(II) species in the reaction is discussed.

Alkylation of Nitrocyanamide. A New Synthesis of Isocyanates

Boyer, Joseph H.,Manimaran, Thanikavelu,Wolford, Lionel T.

, p. 2137 - 2140 (2007/10/02)

Thirteen alkyl halides (primary, secondary, and tertiary aliphatic including alicyclic, aralkyl, and heteroalkyl systems) and certain non-vicinal dihalides on treatment with silver nitrocyanamide are converted into the corresponding isocyanates (63-95percent).Intermediate alkylnitrocyanamides, spectroscopically detected, thermolysed (-20-80 deg C) to the expected isocyanates.In certain examples silver nitrocyanamide is generated in situ from sodium nitrocyanamide and silver nitrate.Silver nitrocyanamide does not react with cyclopropyl bromide, acetyl chloride, toluene-p-sulphonyl chloride, phenacyl bromide and 2-bromomethyldioxolane (27), and the ethylene acetal (28) of 1-bromo-4-iodopentacyclo-nonan-9-one.Silver nitrocyanamide reacts with 4,6-bis(bromomethyl)-3,7-dimethyl-1,5-diazabicyclo3.3.0)octane-2,8-dione (26), to give an intractable mixture.Vicinal dihalides give erratic results without detectable formation of vicinal di-isocyanates: unisolated 2-bromoethyl isocyanate (tentative assignment) has been detected in a product mixture from ethylene dibromide; an expected rearrangement during the reaction with 1,2-dibromocyclobutane, brought about the formation of 4-bromobut-3-enyl isocyanate isolated as ethyl 4-bromobut-3-enylcarbamate in low yield; and 1,2-dibromocyclohexane gives 2-bromocyclohexyl isocyanate isolated as ethyl N-(2-bromocyclohexyl)-carbamate in low yield.

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