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58886-34-3

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58886-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58886-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,8 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58886-34:
(7*5)+(6*8)+(5*8)+(4*8)+(3*6)+(2*3)+(1*4)=183
183 % 10 = 3
So 58886-34-3 is a valid CAS Registry Number.

58886-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylmethoxypropan-2-yloxymethylbenzene

1.2 Other means of identification

Product number -
Other names 2,2-dibenzyloxypropane

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:58886-34-3 SDS

58886-34-3Relevant articles and documents

Lymph-Node-Targeted Immune Activation by Engineered Block Copolymer Amphiphiles-TLR7/8 Agonist Conjugates

Van Herck, Simon,Deswarte, Kim,Nuhn, Lutz,Zhong, Zifu,Portela Catani, Joao Paulo,Li, Yupeng,Sanders, Niek N.,Lienenklaus, Stefan,De Koker, Stefaan,Lambrecht, Bart N.,David, Sunil A.,De Geest, Bruno G.

, p. 14300 - 14307 (2018)

Small molecule immuno-modulators such as agonists of Toll-like receptors (TLRs) are attractive compounds to stimulate innate immune cells toward potent antiviral and antitumor responses. However, small molecules rapidly enter the systemic circulation and

Interception of deaminatively generated benzyl carbenium ions by acetone

Song, Fenhong,Darbeau, Ron W.,White, Emil H.

, p. 1825 - 1829 (2007/10/03)

Essentially free benzyl carbenium ions were generated via protonation of phenyldiazomethane with benzoic acid in acetone. Interestingly, no proton transfer occurred below -20 °C. After protonation and dediazoniation of the diazoalkane at -20 °C, the solvent was found to intercept the deaminatively generated carbocations to yield initially the corresponding O-benzyl oxonium ion and benzyl benzoate. The onium ion, however, was labile under the reaction conditions, and decomposed into a cascade of products whose concentrations as a function of time were used to trace the reaction pathway. Thus, the O-benzyl oxonium ion reacted with benzoate ion to yield (2- benzyloxy)isopropyl benzoate; subsequent decomposition of this O-benzyl-O- benzoyl ketal produced 2,2-dibenzyloxypropane (a dibenzyl ketal), 2- benzyloxypropene, and benzyl alcohol. In a related study, benzyl cations were generated via thermolyses of N-benzyl-N-nitroso-O-benzoyl hydroxylamine at 0 and -70 °C. The product distributions were found to be temperature-dependent and different from that in the PhCHN2 + PhCO2H case.

Topical mosquito repellents. 3. Carboxamide acetals and ketals and related carbonyl addition derivatives.

Tsakotellis,Johnson,Skinner,Skidmore,Maibach

, p. 84 - 89 (2007/10/09)

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