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108103-44-2

Benzenamine, 3,5-dimethoxy-N,N-bis(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108103-44-2

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108103-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108103-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,1,0 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108103-44:
(8*1)+(7*0)+(6*8)+(5*1)+(4*0)+(3*3)+(2*4)+(1*4)=82
82 % 10 = 2
So 108103-44-2 is a valid CAS Registry Number.

108103-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethoxy-N,N-di(propan-2-yl)aniline

1.2 Other means of identification

Product number -
Other names -

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:108103-44-2 SDS

108103-44-2Downstream Products

108103-44-2Relevant articles and documents

Formal synthesis of angiogenesis inhibitor NM-3

Bauta, William E.,Lovett, Dennis P.,Cantrell Jr., William R.,Burke, Brian D.

, p. 5967 - 5973 (2007/10/03)

We report the formal synthesis of angiogenesis inhibitor NM-3 (1) in six steps from either of the 2,4-dimethoxyhalobenzenes 13a,b or 3,5-dimethoxychlorobenzene (13c). The first key reaction is the regiospecific alkylation/rearrangement between the aryne derived from 13a-c with sodium diethylmalonate in THF to produce diester 11, which after hydrolysis and cyclization affords homophthalic anhydride 3. The second is the reaction of anhydride 3 with either ethyl 2-methylmalonate (28a), in the presence of 1,1′-carbonyldiimidazole, or ethyl-2-methylmalonyl chloride (28b) under basic conditions to afford key isocoumarin 27. The conversion of 27 constitutes a formal synthesis of NM-3.

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