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1,3-Propanediol, 2-methyl-2-[(triphenylmethoxy)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96917-84-9

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96917-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96917-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,9,1 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96917-84:
(7*9)+(6*6)+(5*9)+(4*1)+(3*7)+(2*8)+(1*4)=189
189 % 10 = 9
So 96917-84-9 is a valid CAS Registry Number.

96917-84-9SDS

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 2-methyl-2-(trityloxymethyl)propane-1,3-diol

1.2 Other means of identification

Product number -
Other names 1,3-Propanediol,2-methyl-2-[(triphenylmethoxy)methyl]

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:96917-84-9 SDS

96917-84-9Relevant academic research and scientific papers

Self-organized lipid-porphyrin bilayer membranes in vesicular form: Nanostructure, photophysical properties, and dioxygen coordination

Komatsu, Teruyuki,Moritake, Miho,Nakagawa, Akito,Tsuchida, Eishun

, p. 5469 - 5480 (2002)

An amphiphilic tetraphenylporphyrin and its iron complex bearing four phospholipid substituents, in which a trimethylolethane residue connects the two acyl chains (lipid-porphyrins), have been synthesized. The free-base lipid-porphyrin 6a self-organizes i

Stereoarrays with an all-carbon quaternary center: Diastereoselective desymmetrization of prochiral malonaldehydes

Linclau, Bruno,Cini, Elena,Oakes, Catherine S.,Josse, Solen,Light, Mark,Ironmonger, Victoria

supporting information; experimental part, p. 1232 - 1235 (2012/03/11)

Tamed by chelation: The MgBr2 chelation of prochiral malonaldehydes allows diastereoselective monoaddition reactions with allyl stannane nucleophiles (see scheme; PG=protecting group, TBDMS=tert- butyldiphenylmethylsilyl, Tr=trityl). In the same pot, addition of a second nucleophile proceeds in high diastereoselectivity to generate nonsymmetric products with up to five contiguous stereogenic centers, including a chiral all-carbon quaternary center. Copyright

Mettalophtalocyanine dimers incorporating five-atom covalent bridges

Leznoff, Clifford C.,Marcuccio, Sebastian M.,Greenberg, Shafrira,Lever, A. B. P.,Tomer, Kenneth B.

, p. 623 - 631 (2007/10/02)

Metal-free copper and cobalt(II) binuclear phtalocyanines, in which the two phtalocyanine nuclei are covalently linked through five-atom bridges, have been prepared and characterized.Some new metal-free, copper, cobalt(II), and zinc 2,9,16,23-tetraalkoxyp

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