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5-methoxy-2-methyl-2-(4-methylpent-3-en-1-yl)-7-pentyl-2H-chromene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57412-30-3

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57412-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57412-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,1 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57412-30:
(7*5)+(6*7)+(5*4)+(4*1)+(3*2)+(2*3)+(1*0)=113
113 % 10 = 3
So 57412-30-3 is a valid CAS Registry Number.

57412-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxy-2-methyl-2-(4-methylpent-3-enyl)-7-pentylchromene

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:57412-30-3 SDS

57412-30-3Downstream Products

57412-30-3Relevant academic research and scientific papers

A new approach to dl-cannabichromene

Yamaguchi,Shouji,Kuroda

, p. 305 - 308 (2007/10/02)

Natural dl-cannabichromene was synthesized in 6 steps from methyl 5-methoxy-2-methyl-7-pentyl-2H-chromen-2-acetate prepared by the cyclization of 2-hydroxy-6-methoxy-4-pentylbenzaldehyde with dimethyl isopropylidenemalonate.

Synthesis of (+/-)-O-Methylcannabichromene and Some Homologues

de la Torre, M.,Garcia, F.,Cruz, R

, p. 1251 - 1252 (2007/10/02)

A facile novel synthesis of (+/-)-O-methylcannabichromene (5d) together with (+/-)-2-methyl-2-(4-methyl-3-pentenyl)-5-methoxy-2H-benzopyran (5a) and its 7-methyl (5b) and 7-propyl (5c) homologues, using organolithium salts is described.

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