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161469-43-8

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161469-43-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161469-43-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,4,6 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 161469-43:
(8*1)+(7*6)+(6*1)+(5*4)+(4*6)+(3*9)+(2*4)+(1*3)=138
138 % 10 = 8
So 161469-43-8 is a valid CAS Registry Number.

161469-43-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-3-[tert-butyl(diphenyl)silyl]oxypropane-1,2-diol

1.2 Other means of identification

Product number -
Other names 1-O-[(tert-butyl)diphenylsilyl]-sn-glycerol

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:161469-43-8 SDS

161469-43-8Relevant articles and documents

TRANSLOCATION CONTROL ELEMENTS, REPORTER CODES, AND FURTHER MEANS FOR TRANSLOCATION CONTROL FOR USE IN NANOPORE SEQUENCING

-

, (2020/12/07)

Phosphoramidate-based monomers are provided for use in the synthesis of expandable polymers for nanopore-based sensing. Such monomers comprising a reporter construct that contain a first reporter code, a symmetrical chemical brancher bearing a translocati

Carbohydrate-Catalyzed Enantioselective Alkene Diboration: Enhanced Reactivity of 1,2-Bonded Diboron Complexes

Fang, Lichao,Yan, Lu,Haeffner, Fredrik,Morken, James P.

supporting information, p. 2508 - 2511 (2016/03/12)

Catalytic enantioselective diboration of alkenes is accomplished with readily available carbohydrate-derived catalysts. Mechanistic experiments suggest the intermediacy of 1,2-bonded diboronates.

Synthesis of novel, fluorescently tagged analogs of glycosylphosphatidylinositol (GPI) anchors

Johnson, Charles L.,Guo, Zhongwu

, p. 301 - 323 (2013/10/08)

Glycosylphosphatidylinositol (GPI) anchors are a group of complex glycolipids that attach extracellular proteins and glycoproteins to the eukaryotic cell outer membrane. To better understand GPI anchorage, it is necessary to have access to homogeneous, structurally defined, and functionalized GPIs and GPI analogs. In this regard, chemical synthesis is necessary, as GPI anchors are rather scarce and heterogeneous in natural sources. Three GPI analogs with phosphoglycerolipids linked to the pseudodisaccharide core and their fluorescein conjugates were prepared in this work as a small tool set useful for probing how the lipid composition and carbohydrate anomeric configuration may affect the properties of GPI anchors.

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