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4272-07-5

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4272-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4272-07-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4272-07:
(6*4)+(5*2)+(4*7)+(3*2)+(2*0)+(1*7)=75
75 % 10 = 5
So 4272-07-5 is a valid CAS Registry Number.

4272-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name CbzNHC11H22CO2H

1.2 Other means of identification

Product number -
Other names 12-benzyloxycarbonylaminododecanoic acid

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:4272-07-5 SDS

4272-07-5Relevant articles and documents

Molecular monolayer nanotubes having 7-9 nm inner diameters covered with different inner and outer surfaces

Kameta, Naohiro,Mizuno, Go,Masuda, Mitsutoshi,Minamikawa, Hiroyuki,Kogiso, Masaki,Shimizu, Toshimi

, p. 896 - 897 (2007)

Novel unsymmetrical bolaamphiphile, bearing glucose- and triglycine-headgroups at both ends, exclusively self-assembled into nanotubes with 7-9-nm inner diameters, which consist of a single monolayer lined by polyglycine-II-type hydrogen-bond networks among the triglycine moieties. Copyright

COMPOUND OR SALT THEREOF, NATURAL KILLER T CELL ACTIVATOR, AND PHARMACEUTICAL COMPOSITION

-

Paragraph 0088-0090, (2020/07/16)

The invention provides a compound or a salt thereof capable of activating natural killer T cell, a natural killer T cell activating agent containing such a compound or a salt thereof, and a pharmaceutical composition. The compound of the invention is a co

Supramolecular hydrogel formed by glucoheptonamide of l-lysine: simple preparation and excellent hydrogelation ability

Suzuki, Masahiro,Owa, Sanae,Shirai, Hirofusa,Hanabusa, Kenji

, p. 7302 - 7308 (2008/02/05)

We describe the simple preparation of new l-lysine derivatives with a gluconic or glucoheptonic group, their hydrogelation properties, and the thermal and mechanical properties of the supramolecular hydrogels. The l-lysine derivatives with a gluconic group have no hydrogelation ability, while the l-lysine-glucoheptonamide derivatives functioned as hydrogelators. Their hydrogelation abilities increased with the decreasing length of the spacer between the l-lysine segment and the glucoheptonic group. The compound, which has no spacer, formed a supramolecular hydrogel at 0.05 wt % in pure water. The thermal stability and high mechanical strength of the supramolecular hydrogels based on this compound significantly depended on the aqueous solutions. Electron microscopy and FTIR studies demonstrated?that the hydrogelators created a three-dimensional network through hydrogen bonding and hydrophobic interactions in the supramolecular hydrogel. In addition, it was found that hydrophobic interactions played an important role in the thermal stability of the supramolecular hydrogel.

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