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85359-61-1

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85359-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85359-61-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,5 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 85359-61:
(7*8)+(6*5)+(5*3)+(4*5)+(3*9)+(2*6)+(1*1)=161
161 % 10 = 1
So 85359-61-1 is a valid CAS Registry Number.

85359-61-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name chalaurenol

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:85359-61-1 SDS

85359-61-1Upstream product

85359-61-1Downstream Products

85359-61-1Relevant articles and documents

PHOTOOXYGENATION OF 2',4,4'-TRIHYDROXYCHALCONE: IDENTITY WITH PRODUCTS FROM ENZYMIC OXIDATION

Wong, Edmon

, p. 1544 - 1545 (2007/10/02)

The dioxetane derivative of 2',4,4'-trihydroxychalcone, previously known as a product from peroxidase-catalysed oxidation, has now been detected in the dye-sensitized photooxygenation of the same chalcone and shown to be accountable for the host of other products formed. - Key Word Index: Dioxetanes; chalcones; photooxygenation.

Chalaurenol: a Novel Product from Enzymic Oxidation of 2',4,4'-Trihydroxychalcone

Begley, Michael J.,Crombie, Leslie,London, Martin,Savin, John,Whiting, Donald A.

, p. 1319 - 1321 (2007/10/02)

Peroxidase enzymes from various sources convert 2',4,4'-trihydroxychalcone (1) into the novel quinol ether of 2-formyl-6-hydroxycoumaranone (6), the structure of which was determined by X-ray diffraction; a biosynthetic pathway is suggested and capillarisin (11) may arise by a similar route.

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