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7,8-dihydroxy-6-methyl-4-propan-2-yl-naphthalene-1,2-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74635-95-3

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74635-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74635-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,3 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74635-95:
(7*7)+(6*4)+(5*6)+(4*3)+(3*5)+(2*9)+(1*5)=153
153 % 10 = 3
So 74635-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H14O4/c1-6(2)8-5-10(15)13(17)11-9(8)4-7(3)12(16)14(11)18/h4-6,16,18H,1-3H3

74635-95-3SDS

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 7,8-dihydroxy-6-methyl-4-propan-2-ylnaphthalene-1,2-dione

1.2 Other means of identification

Product number -
Other names 7,8-DIHYDROXY-6-METHYL-4-PROPAN-2-YL-NAPHTHALENE-1,2-DIONE

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:74635-95-3 SDS

74635-95-3Downstream Products

74635-95-3Relevant academic research and scientific papers

Naturally Occurring Quinones. Part 28. Sesquiterpenoid Quinones and Related Compounds from Hibiscus tiliaceus

Ali, Sadaquat,Singh, Pahup,Thomson, Ronald H.

, p. 257 - 259 (2007/10/02)

The heartwood of H. tiliaceus is red and fades on exposure to light.Like H. elatus heartwood, which behaves similarly, it contains hibiscones A - D and hibiscoquinones A - D; one sample which was devoid of red pigments contained lapachol while roots (from Brazil) contained gossypol, and mansonones D and F.Hibiscoquinone B can be obtained from hibiscones C and D by autoxidation in alkaline solution, and the formation of other hibiscoquinones can be accounted for by related processes.It is suggested that the hibiscoquinones are derived in vivo from the hibiscones.

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