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9-((2-hydroperoxy-3-methyl-3-butenyl)oxy)-7H-furo(3,2-g)(1)benzopyran-7-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135366-51-7

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135366-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135366-51-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,3,6 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 135366-51:
(8*1)+(7*3)+(6*5)+(5*3)+(4*6)+(3*6)+(2*5)+(1*1)=127
127 % 10 = 7
So 135366-51-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O6/c1-9(2)12(22-18)8-20-16-14-11(5-6-19-14)7-10-3-4-13(17)21-15(10)16/h3-7,12,18H,1,8H2,2H3

135366-51-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(2-hydroperoxy-3-methylbut-3-enoxy)furo[3,2-g]chromen-7-one

1.2 Other means of identification

Product number -
Other names 9-[(2-hydroperoxy-3-methylbut-3-en-1-yl)oxy]-7h-furo[3,2-g]chromen-7-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:135366-51-7 SDS

135366-51-7Upstream product

135366-51-7Downstream Products

135366-51-7Relevant academic research and scientific papers

Photosynthesis of furocoumarin- and furochromone-types potential intercalative alkylating and oxidizing agents of dna through photooxidations using γ-ray

Elgendy,Ramadan,Fadaly,Hammouda

, p. 434 - 437 (2007/10/03)

The photooxygenation of imperatorin (1a) under γ-ray irradiation afforded the hydroperoxides 2a and 3a. Similarly, the photooxygenation of alloimperatorin (1b) gave the hydroperoxide (2b). Visnagin (1c) was also photooxygenated to give the hydroperoxide (2c) as sole product. On the other hand, the photooxygenation of khellin (1d) gave the endoperoxide (2d) as a sole product. The epoxidation of imperatorin (1a) using hydrogen peroxide under γ-ray irradiation afforded the epoxide 5a. Similarly visnagin (1c) and khellin (1d) were epoxidized to give the epoxides 5c and 5d.

Photooxygenation of Some Potentially Skin-Photosensitizing Furocoumarins: Imperatorin, Alloimperatorin and Its Methyl Ester and Acetate Derivatives

Abou-Elzahab, Mohamed M.,Adam, Waldemar,Saha-Moeller, Chantu R.

, p. 967 - 970 (2007/10/02)

The photooxygenation of imperatorin (1a) afforded the corresponding allylic hydroperoxides 2a and 3a in very good yields.Similarly, the photooxygenation of alloimperatorin derivatives 1c, d gave the allylic hydroperoxides 2c, d and 3c, d in quantitative yields.On the other hand, on photooxygenation of alloimperatorin (1b) exclusively the dienone hydroperoxide 4b was obtained.When the reaction time was prolonged, the bis(hydroperoxide) 5b was also formed by successive photooxygenation of 4b. Key Words: Photooxygenation / Hydroperoxides, allylic / Singlet oxygen / Furocoumarins / Imperatorin / Alloimperatorin

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