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807364-49-4

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807364-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 807364-49-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,7,3,6 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 807364-49:
(8*8)+(7*0)+(6*7)+(5*3)+(4*6)+(3*4)+(2*4)+(1*9)=174
174 % 10 = 4
So 807364-49-4 is a valid CAS Registry Number.

807364-49-4SDS

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 1-(4'-nitrophenyl)-1-hydroxy-5-methoxy-3-pentanone

1.2 Other means of identification

Product number -
Other names 1-hydroxy-5-methoxy-1-(4-nitrophenyl)pentan-3-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:807364-49-4 SDS

807364-49-4Relevant articles and documents

Efficient Baylis-Hillman reactions of cyclic enones in methanol as catalyzed by methoxide anion

Luo, Sanzhong,Mi, Xueling,Xu, Hui,Wang, Peng George,Cheng, Jin-Pei

, p. 8413 - 8422 (2007/10/03)

The Baylis-Hillman reactions of cyclic enones with a variety of aldehydes were investigated. 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) was found to be a viable catalyst in promoting the reactions of sterically retarded substrates in methanol. The reactions showed clear solvent dependence and only occurred in hydroxylic solvents, especially in methanol. Further consideration on the steric character of DBU and its high basicity jointly with other experimental observations suggests that the methoxide anion should be the "true" Baylis-Hillman catalyst. This has been confirmed by the effectiveness of similar reactions directly employing methoxide as the catalyst. The reaction pathways of this type of catalysis are proposed to depend on the choice of substrates. Supporting experimental observations were demonstrated and discussed in relation to mechanistic considerations. This study also reveals that both DBU and sodium methoxide can be successfully applied as effective catalysts in methanol to promote the Baylis-Hillman reactions for a range of cyclic enones including cyclopent-2-enones, cyclohex-2-enones, γ-pyrone, and 1-benzopyran-4(4H)- ones.

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