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hexadecyl carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54850-40-7

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54850-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54850-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,5 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54850-40:
(7*5)+(6*4)+(5*8)+(4*5)+(3*0)+(2*4)+(1*0)=127
127 % 10 = 7
So 54850-40-7 is a valid CAS Registry Number.

54850-40-7SDS

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 hexadecyl carbamate

1.2 Other means of identification

Product number -
Other names Carbamidsaeure-hexadecylester

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:54850-40-7 SDS

54850-40-7Downstream Products

54850-40-7Relevant academic research and scientific papers

Aziridination of C60 with simple amides and catalytic rearrangement of the aziridinofullerenes to azafulleroids

Tsuruoka, Ryoji,Nagamachi, Toshiki,Murakami, Yuta,Komatsu, Mitsuo,Minakata, Satoshi

supporting information; experimental part, p. 1691 - 1697 (2009/07/30)

The selective formation of aziridinofullerene and azafulleroid, which are isomers of the fullerene derivatives-introduced N1 unit, is achieved. The ionic aziridination is a very convenient and risk-free procedure compared with the conventional

Process for the preparation of asymmetrically substituted ureas, carbamates or thiocarbamates

-

, (2008/06/13)

Process for the preparation of asymmetrically substituted ureas, carbamates, thiocarbamates or substituted isocyanates by reaction of an adduct of isocyanic acid and a tertiary amine with a primary and secondary amine, an alcohol, a thiol or a compound having one or two non-cumulated olefinic double bonds, and a process for the preparation of N-mono- or N,N-disubstituted ureas by reaction of ammonium isocyanate with a primary or secondary amine in a diluent.

Process for the preparation of substituted isocyanates

-

, (2008/06/13)

Process for the preparation of asymmetrically substituted ureas, carbamates, thiocarbamates or substituted isocyanates by reaction of an adduct of isocyanic acid and a tertiary amine with a primary and secondary amine, an alcohol, a thiol or a compound having one or two non-cumulated olefinic double bonds.

Photochemistry of reactive surface-active compounds in adsorbed monolayers

Holden, David A.,Taylor, Joseph W.,Clausen, Diane

, p. 1671 - 1678 (2007/10/02)

The reactions of long-chain diazo ketones and azides in adsorbed monolayers on inorganic solids were investigated and compared with the corresponding behaviour in monolayers at the air-water interface. The isolated products indicate that reaction of photochemically generated intermediates occurs both with co-adsorbed water and with hydroxyl groups on the solid surface. In the case of 1-diazo-2-oxoheptadecane, for example, the products of these two reactions are heptadecanoic acid and a surface-grafted long-chain ester. The latter can be removed as methyl heptadecanoate by ester exchange using methanolic HCl. Pronounced differences were observed between alumina, silica gel and fumed silica as supports, and were attributed to differences in the amount of adsorbed H2O and in the density of surface hydroxyl groups.

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