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CYCLOPROPYL 4-METHOXYDIPHENYLCARBINOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62587-03-5

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62587-03-5 Usage

Chemical Properties

clear light yellow viscous liquid after melting

Check Digit Verification of cas no

The CAS Registry Mumber 62587-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,8 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62587-03:
(7*6)+(6*2)+(5*5)+(4*8)+(3*7)+(2*0)+(1*3)=135
135 % 10 = 5
So 62587-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H18O2/c1-19-16-11-9-15(10-12-16)17(18,14-7-8-14)13-5-3-2-4-6-13/h2-6,9-12,14,18H,7-8H2,1H3/t17-/m0/s1

62587-03-5SDS

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 (R)-cyclopropyl-(4-methoxyphenyl)-phenylmethanol

1.2 Other means of identification

Product number -
Other names dl-Cyclopropyl-4-anisyl-phenylcarbinol

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:62587-03-5 SDS

62587-03-5Relevant academic research and scientific papers

Hydride Reduction by a Sodium Hydride-Iodide Composite

Too, Pei Chui,Chan, Guo Hao,Tnay, Ya Lin,Hirao, Hajime,Chiba, Shunsuke

supporting information, p. 3719 - 3723 (2016/03/26)

Sodium hydride (NaH) is widely used as a Br?nsted base in chemical synthesis and reacts with various Br?nsted acids, whereas it rarely behaves as a reducing reagent through delivery of the hydride to polar π electrophiles. This study presents a series of reduction reactions of nitriles, amides, and imines as enabled by NaH in the presence of LiI or NaI. This remarkably simple protocol endows NaH with unprecedented and unique hydride-donor chemical reactivity.

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