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65473-81-6

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65473-81-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65473-81-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,7 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65473-81:
(7*6)+(6*5)+(5*4)+(4*7)+(3*3)+(2*8)+(1*1)=146
146 % 10 = 6
So 65473-81-6 is a valid CAS Registry Number.

65473-81-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-epoxy-3-methyl-1-phenyl-butane

1.2 Other means of identification

Product number -
Other names 1,2-Epoxy-3-methyl-1-phenyl-butan

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:65473-81-6 SDS

65473-81-6Relevant articles and documents

Kinetic resolution ofN-aryl β-amino alcoholsviaasymmetric aminations of anilines

Guo, Zheng,Xie, Jinglei,Hu, Tao,Chen, Yunrong,Tao, Houchao,Yang, Xiaoyu

supporting information, p. 9394 - 9397 (2021/09/22)

An efficient kinetic resolution ofN-aryl β-amino alcohols has been developedviaasymmetricpara-aminations of anilines with azodicarboxylates enabled by chiral phosphoric acid catalysis. Broad substrate scope and high kinetic resolution performances were afforded with this method. Control experiments supported the critical roles of the NH and OH group in these reactions.

Process for the preparation of an oxirane, azirdine or cyclopropane

-

, (2008/06/13)

A process for the preparation of an oxirane, aziridine or cyclopropane of formula (I) wherein, X is oxygen, NR4 or CHR5 ; R1 is hydrogen, alkyl, aryl, heteroaromatic, heterocyclic or cycloalkyl; R2 is hydrogen, alkyl, aryl, heteroaromatic, CO2 R8, CHR14 NHR13, heterocyclic or cycloalkyl; or R1 and R2 join together to form a cycloalkyl ring; R3 is hydrogen, alkyl, aryl, heteroaromatic, CO2 R8, R83 Sn, CONR8 R9 or trimethylsilyl; R4 and R5 are, independently, alkyl, cycloalkyl, aryl, heteroaromatic, SO2 R8, SO3 R8, COR8, CO2 R8, CONR8 R9 or CN, or R4 can also be P(O)(aryl)2 ; R8 and R9 are independently alkyl, aryl or arylalkyl; R13 and R14 are independently hydrogen, alkyl or aryl; the process comprising reacting a mixture of a compound of formula (II), wherein R1, R2 and X are as defined above, and a sulphide of formula SR6 R7, wherein R6 and R7 are independently alkyl, aryl or heteroaomatic, or R6 and R7 join together to form a cycloalkyl ring which optionally includes an additional heteroatom, with either (i) a metallocarbon obtainable by reacting an alkylmetal with a methane derivative of formula CHR3 X'X", wherein R3 is as defined above, and X' and X" are independently, a leaving group, or (ii) a metallocarbon obtainable by reacting a compound of formula (III), (wherein R3 may not be hydrogen) with a suitable organometallic or inorganic reagent.

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