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4850-49-1

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4850-49-1 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 93, p. 6313, 1971 DOI: 10.1021/ja00752a078The Journal of Organic Chemistry, 49, p. 1589, 1984 DOI: 10.1021/jo00183a020Tetrahedron, 36, p. 299, 1980 DOI: 10.1016/0040-4020(80)80018-4

Check Digit Verification of cas no

The CAS Registry Mumber 4850-49-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,5 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4850-49:
(6*4)+(5*8)+(4*5)+(3*0)+(2*4)+(1*9)=101
101 % 10 = 1
So 4850-49-1 is a valid CAS Registry Number.

4850-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenylpropane-1,3-diol

1.2 Other means of identification

Product number -
Other names 3-hydroxy-1-phenyl-1-propanol

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:4850-49-1 SDS

4850-49-1Relevant articles and documents

KB3H8: An environment-friendly reagent for the selective reduction of aldehydes and ketones to alcohols

Li, Xinying,Mi, Tongge,Guo, Wenjing,Ruan, Zhongrui,Guo, Yu,Ma, Yan-Na,Chen, Xuenian

, p. 12776 - 12779 (2021/12/10)

Selective reduction of aldehydes and ketones to their corresponding alcohols with KB3H8, an air- and moisture-stable, nontoxic, and easy-to-handle reagent, in water and THF has been explored under an air atmosphere for the first time. Control experiments illustrated the good selectivity of KB3H8 over NaBH4 for the reduction of 4-acetylbenzaldehyde and aromatic keto esters. This journal is

4CzIPN catalyzed photochemical oxidation of benzylic alcohols

Zhang, Heng,Guo, Tianyun,Wu, Mingzhong,Huo, Xing,Tang, Shouchu,Wang, Xiaolei,Liu, Jian

supporting information, (2021/02/20)

A green photoredox oxidation of benzylic primary and secondary alcohols to aldehydes and ketones with air as an oxidant was reported. The oxidation shows broad substrate scope and excellent selectivity over benzylic alcohols to the aliphatic alcohols. Further mechanistic studies revealed a quinuclidine mediated HAT process, and blue LEDs promoted 4CzlPN (1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene) photoredox cycle were involved in our oxidation.

Deoxyfluorination with CuF2: Enabled by Using a Lewis Base Activating Group

Bode, Bela E.,Chabbra, Sonia,Champion, Sue,Dawson, Daniel M.,Sood, D. Eilidh,Sutherland, Andrew,Watson, Allan J. B.

supporting information, p. 8460 - 8463 (2020/04/10)

Deoxyfluorination is a primary method for the formation of C?F bonds. Bespoke reagents are commonly used because of issues associated with the low reactivity of metal fluorides. Reported here is the development of a simple strategy for deoxyfluorination, using first-row transition-metal fluorides, and it overcomes these limitations. Using CuF2 as an exemplar, activation of an O-alkylisourea adduct, formed in situ, allows effective nucleophilic fluoride transfer to a range of primary and secondary alcohols. Spectroscopic investigations have been used to probe the origin of the enhanced reactivity of CuF2. The utility of the process in enabling 18F-radiolabeling is also presented.

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