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135266-95-4

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  • 4-Nitrophenyl 2-(Acetylamino)-2-deoxy-α-D-galactopyranoside 3,4,6-Triacetate

    Cas No: 135266-95-4

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135266-95-4 Usage

Chemical Properties

Yellow Syrup

Uses

4-Nitrophenyl 2-(Acetylamino)-2-deoxy-α-D-galactopyranoside 3,4,6-Triacetate (cas# 135266-95-4) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 135266-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,2,6 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 135266-95:
(8*1)+(7*3)+(6*5)+(5*2)+(4*6)+(3*6)+(2*9)+(1*5)=134
134 % 10 = 4
So 135266-95-4 is a valid CAS Registry Number.

135266-95-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3R,4R,5R,6R)-5-acetamido-3,4-diacetyloxy-6-(4-nitrophenoxy)oxan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names 4-Nitrophenyl 2-(Acetylamino)-2-deoxy-|A-D-galactopyranoside 3,4,6-Triacetate

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:135266-95-4 SDS

135266-95-4Downstream Products

135266-95-4Relevant articles and documents

Synthesis and Characterization of Versatile O-Glycan Precursors for Cellular O-Glycomics

Zhang, Qing,Li, Zhonghua,Chernova, Tatiana,Saikam, Varma,Cummings, Richard,Song, Xuezheng,Ju, Tongzhong,Smith, David F.,Wang, Peng G.

, p. 2507 - 2513 (2019/11/13)

Protein O-glycosylation is a universal post-translational modification and plays essential roles in many biological processes. Recently we reported a technology termed cellular O-glycome reporter/amplification (CORA) to amplify and profile mucin-type O-glycans of living cells growing in the presence of peracetylated Benzyl-α-GalNAc (Ac3GalNAc-α-Bn). However, the application and development of the CORA method are limited by the properties of the precursor benzyl aglycone, which is relatively inert to further chemical modifications. Here we described a rapid parallel microwave-assisted synthesis of Ac3GalNAc-α-Bn derivatives to identify versatile precursors for cellular O-glycomics. In total, 26 derivatives, including fluorescent and bioorthogonal reactive ones, were successfully synthesized. The precursors were evaluated for their activity as acceptors for T-synthase and for their ability to function as CORA precursors. Several of the precursors possessing useful functional groups were more efficient than Ac3GalNAc-α-Bn as T-synthase acceptors and cellular O-glycome reporters. These precursors will advance the CORA technology for studies of functional O-glycomics.

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