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1(2H)-Naphthalenone, 2-(1,1-dimethylethyl)-2-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103768-75-8

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103768-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103768-75-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,6 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103768-75:
(8*1)+(7*0)+(6*3)+(5*7)+(4*6)+(3*8)+(2*7)+(1*5)=128
128 % 10 = 8
So 103768-75-8 is a valid CAS Registry Number.

103768-75-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-2-tert-butyl-1-naphthalenone

1.2 Other means of identification

Product number -
Other names 2-Benzyl-2-tert-butyl-2H-naphthalen-1-one

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:103768-75-8 SDS

103768-75-8Downstream Products

103768-75-8Relevant academic research and scientific papers

Formation and Rearrangement of 8a-Benzyl-2-tert-butyl-1(8aH)-naphthalenone, a Ketone with a Ring System Consisting Entirely of Fused Blocked Aromatic Rings

Miller, Bernard,Baghdadchi, Jamil

, p. 3390 - 3394 (2007/10/02)

The dibromobicyclic ketone 5 was synthesized by a three-step process starting with 2-tert-butyl-1-naphthol.Dehydrobromination of 5 by reaction with DBU resulted in isolation of the 1-naphthalenone 7.Formation of 7 is attributed to a shift in the int

An Extraordinarily Rapid Benzyl Shift in a Molecule with a Ring System consisting Entirely of Fused Blocked Aromatic Rings

Miller, Bernard,Baghdadchi, Jamil

, p. 511 - 512 (2007/10/02)

Dehydrobromination of the dibromobicyclic ketone (4) at 0 deg C resulted in the formation of ketone (5); the remarkably rapid benzyl shift in this reaction is attributed to formation and rearrangement of ketone (2), a unique example of a molecule wi

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