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1H-Cyclopropa[b]naphthalene, 3,6-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

153202-79-0

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153202-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153202-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,2,0 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 153202-79:
(8*1)+(7*5)+(6*3)+(5*2)+(4*0)+(3*2)+(2*7)+(1*9)=100
100 % 10 = 0
So 153202-79-0 is a valid CAS Registry Number.

153202-79-0SDS

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 3,6-dimethoxy-1H-cyclopropa[b]naphthalene

1.2 Other means of identification

Product number -
Other names 1H-Cyclopropa[b]naphthalene,3,6-dimethoxy

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:153202-79-0 SDS

153202-79-0Downstream Products

153202-79-0Relevant academic research and scientific papers

Studies in the Cycloproparene Series: Unexpected Products from Peterson Olefinations

Halton, Brian,Boese, Roland,Dixon, Gareth M.

, p. 4507 - 4512 (2007/10/03)

Reaction of tetraphenylcyclopentadienone with anion 8 derived by monodesilylation of 1,1-bis(trimethylsilyl)cyclopropa[b]naphthalene (10) gives the 1-(5′-cyclopentadienyl)-substituted cycloproparene 17 from simple anion addition to the carbonyl group rather than fulvalene 16 from loss of Me3SiO-. Reactions of anion 8 with p-(trifluoromethyl)benzaldehyde and thiophene-2-carbaldehyde give the expected exocyclic olefins 12a and 12b, respectively. In contrast, the 3,6-dimethoxy analogue 24, obtained from cycloproparene 20, gives the C1 unsubstituted cycloproparene 19 and the Tishchenko products, p-(trifluoromethyl)benzyl p-(trifluoromethyl)benzoate (21) and 2-thienylmethyl thiophene-2-carboxylate (22), respectively. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

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