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61949-16-4

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61949-16-4 Usage

General Description

N-Benzoyl-D-glucosamine is a chemical compound that is derived from glucosamine, a naturally occurring amino sugar found in the human body. It is commonly used in the cosmetic and pharmaceutical industries for its skin-lightening and anti-aging properties. N-Benzoyl-D-glucosamine acts as a potent inhibitor of melanin production, making it effective for treating skin hyperpigmentation and dark spots. Additionally, it has been shown to have moisturizing and anti-inflammatory effects, making it a popular ingredient in skincare products. Overall, N-Benzoyl-D-glucosamine is a versatile compound with various potential applications in the fields of skincare and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 61949-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,4 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61949-16:
(7*6)+(6*1)+(5*9)+(4*4)+(3*9)+(2*1)+(1*6)=144
144 % 10 = 4
So 61949-16-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO6/c15-6-8-10(16)11(17)9(13(19)20-8)14-12(18)7-4-2-1-3-5-7/h1-5,8-11,13,15-17,19H,6H2,(H,14,18)

61949-16-4SDS

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 N-[(2S,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]benzamide

1.2 Other means of identification

Product number -
Other names 2-deoxy-2-benzamido-D-glucopyranose

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:61949-16-4 SDS

61949-16-4Relevant articles and documents

Synthesis of Benzoisoselenazolones via Rh(III)-Catalyzed Direct Annulative Selenation by Using Elemental Selenium

Xu-Xu, Qing-Feng,Nishii, Yuji,Uetake, Yuta,Sakurai, Hidehiro,Miura, Masahiro

supporting information, p. 17952 - 17959 (2021/11/16)

Isoselenazolone derivatives have attracted significant research interest because of their potent therapeutic activities and indispensable applications in organic synthesis. Efficient construction of functionalized isoselenazolone scaffolds is still challenging, and thus new synthetic approaches with improved operational simplicity have been of particular interest. In this manuscript, we introduce a rhodium-catalyzed direct selenium annulation by using stable and tractable elemental selenium. A series of benzamides as well as acrylamides were successfully coupled with selenium under mild reaction conditions, and the obtained isoselenazolones could be pivotal synthetic precursors for several organoselenium compounds. Based on the designed control experiments and X-ray absorption spectroscopy measurements, we propose an unprecedented selenation mechanism involving a highly electrophilic Se(IV) species as the reactive selenium donor. The reaction mechanism was further verified by a computational study.

USE OF UAP INHIBITORS TO INHIBIT FLUX THROUGH THE HEXOSAMINE BIOSYNTHETIC PATHWAY

-

Page/Page column 62; 63, (2016/02/29)

Disclosed are UAP inhibitors to inhibit glucose flux in the hexosamine biohynthetic pathway and methods of treating a disease using the inhibitors.

β-Methyl-2-amino-2,3-didesoxyribofuranoside, a Novel Building Block for Backbone Modified Antisense Oligonucleotides

Winkler, Johannes,Urban, Ernst,Noe, Christian R.

, p. 109 - 116 (2007/10/03)

A synthesis of the amino sugar 2-amino-2,3-didesoxyribose is described. Starting from D-glucosamine, β-methylfuranoside was obtained in eight steps in 20% yield. This carbohydrate is a novel building block for nucleosides and for backbone modified antisense oligonucleotides with 2′-5′ amide linkages.

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