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demethylphytylplastoquinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76448-36-7

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76448-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76448-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,4 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76448-36:
(7*7)+(6*6)+(5*4)+(4*4)+(3*8)+(2*3)+(1*6)=157
157 % 10 = 7
So 76448-36-7 is a valid CAS Registry Number.
InChI:InChI=1/C27H44O2/c1-20(2)10-7-11-21(3)12-8-13-22(4)14-9-15-23(5)16-17-25-24(6)26(28)18-19-27(25)29/h16,18-22H,7-15,17H2,1-6H3/b23-16+/t21-,22-/m1/s1

76448-36-7SDS

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 2-methyl-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enyl]cyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 3-Phytyltoluquinone

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:76448-36-7 SDS

76448-36-7Downstream Products

76448-36-7Relevant academic research and scientific papers

Transformation of 1-(1,2-propadienyl)cyclopropanols into substituted hydroquinones employing octacarbonyldicobalt

Owada, Yufu,Matsuo, Takeshi,Iwasawa, Nobuharu

, p. 11069 - 11086 (2007/10/03)

A novel transformation of 1-(1,2-propadienyl)cyclopropanols into substituted 1,4-hydroquinones has been developed utilizing the interaction of 1,2-propadienes and octacarbonyldicobalt (Co2(CO)8). This reaction was applied to the synthesis of vitamin E and K analogs.

2-METHYL-6-PHYTYLQUINOL AND 2,3-DIMETHYL-5-PHYTYLQUINOL AS PRECURSORS OF TOCOPHEROL SYNTHESIS IN SPINACH CHLOROPLASTS

Soll, Juergen,Shultz, Gernot

, p. 215 - 218 (2007/10/02)

The incorporation of from SAM- into precursors indicates the following sequence of tocopherol synthesis in spinach: 2-methyl-6-phytylquinol (6-phytyltoluquinol) (1a) -> 2,3-dimethyl-5-phytylquinol (phytylplastoquinol) (2a) -> γ-tocopherol (5a) -> α-tocopherol (6). 1a is a particularly preferred to 2-methyl-5-phytylquinol (1b) and 2-methyl-3-phytylquinol (1c). 1a only forms 2a. 2a is converted to 6 via 5a and, to a lesser extent, 2,5-dimethyl-6-phytylquinol (2b) to 6 via β-tocopherol (5b).Trimethylphytylquinol (3) is not an intermediate in the formation of 6.All reactions are independent of light. - Key Word Index - Spinacia oleracea; Chenopodiaceae; tocopherol biosynthesis; 2-methyl-6-phytylquinol; 2,3-dimethyl-phytylquinol; phytylquinol synthesis.

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