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5-bromo-N-[(4-phenyltetrahydro-2H-pyran-4-yl)methyl]furan-2-carboxamide is a complex organic compound with a molecular formula of C18H18BrNO3. It features a furan-2-carboxamide core, which is a heterocyclic structure containing a furan ring and an amide group. The molecule is characterized by the presence of a bromine atom at the 5-position of the furan ring, which imparts specific chemical properties. The amide group is connected to a 4-phenyltetrahydro-2H-pyran-4-ylmethyl moiety, which adds to the structural complexity and potential biological activity of the compound. This chemical is of interest in the field of medicinal chemistry and may have applications in the development of new drugs or as a research tool in chemical biology.

6107-26-2

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6107-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6107-26-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,0 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6107-26:
(6*6)+(5*1)+(4*0)+(3*7)+(2*2)+(1*6)=72
72 % 10 = 2
So 6107-26-2 is a valid CAS Registry Number.

6107-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-N-[(4-phenyloxan-4-yl)methyl]furan-2-carboxamide

1.2 Other means of identification

Product number -
Other names cholesteryl N-phenylcarbamate

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:6107-26-2 SDS

6107-26-2Relevant academic research and scientific papers

Using hydrogen bonding to control carbamate C-N rotamer equilibria

Moraczewski, Alexei L.,Banaszynski, Laura A.,From, Aaron M.,White, Courtney E.,Smith, Bradley D.

, p. 7258 - 7262 (2007/10/03)

In chloroform solution, the syn/anti rotamer ratios for AT-(2-pyridyl)carbamates, 3, and JV-phenylcarbamates, 4, are close to 0.05. Addition of the double hydrogen bonding acetic acid moderately stabilizes the syn rotamer of 4, but has no measurable effec

A CONVENIENT LEWIS ACID CATALYZED PREPARATION OF CARBAMATES FROM SECONDARY ALKOHOLS AND ISOCYANATES

Ibuka, Toshiro,Chu, Gil-Namg,Aoyagi, Takeshi,Kitada, Kazuko,Tsukida, Takahiro,Yoneda, Fumio

, p. 451 - 454 (2007/10/02)

The Lewis acids have been found to be highly effective catalysts for the carbamate formation from secondary alcohols and isocyanates.KEYWORDS - Lewis acid; secondary alcohol; isocyanate; carbamate; γ-carbamoyloxy-α,β-enoate

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