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4-hydroxy-alpha,alpha,4-trimethylcyclohex-2-ene-1-methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57030-53-2

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57030-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57030-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,3 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57030-53:
(7*5)+(6*7)+(5*0)+(4*3)+(3*0)+(2*5)+(1*3)=102
102 % 10 = 2
So 57030-53-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O2/c1-9(2,11)8-4-6-10(3,12)7-5-8/h4,6,8,11-12H,5,7H2,1-3H3

57030-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-p-menth-2-ene-1,8-diol

1.2 Other means of identification

Product number -
Other names trans-p-menth-2-en-1,8-diol

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:57030-53-2 SDS

57030-53-2Relevant academic research and scientific papers

ELECTROPHILIC ADDITION OF LEAD TETRAACETATE TO 2-CARENE IN AN ACIDIDIC MEDIUM

Arbuzov, B. A.,Isaeva, Z. G.,Belyaeva, M. G.,Ratner, V. V.,Kataeva, O. N.,et al.

, p. 117 - 119 (2007/10/02)

Oxidation of 2-carene by lead tetraacetate in acetic acid afforded p-menth-1(10),2-dien-7-ol, 2-acetyl-6,6-dimethylbicyclohexane, p-menth-2-ene-1α,7-diol, p-menth-1-ene-3β,7-diol, and 2-(m-tolyl)propanol-2.Keywords: oxidation, lead tetraacetate, 2-carene, benzene, acetic acid, medium polarity.

Stereoselective Cyclization assisted by the Selenyl Group. Biogenetic-type Synthesis in the p-Menthane Series

Kametani, Tetsuji,Kurobe, Hiroshi,Nemoto, Hideo

, p. 756 - 760 (2007/10/02)

Acid-catalysed cyclization of the β-hydroxyselenide (3), derived from linalyl acetate (1), afforded the trans-p-menthanes (4) and (5), the structures of which were confirmed by their transformation into (6), (11), (8), and (13), and alternative syntheses of these compounds.The structure determination of some products obtained by the reaction of limonene and α-terpineol epoxides with phenylselenium anion was also carried out.

Studies on the stereochemical course of selenium-assisted cyclisation: Biogenetic-type synthesis in the p-menthan series

Kametani, Tetsuji,Kurobe, Hiroshi,Nemoto, Hideo

, p. 762 - 763 (2007/10/02)

Acid-catalysed cyclisation of the β-hydroxy selenide (3) denved from linalyl acetate (1) afforded the trans-p-methans (4) and (5), the structures of which were confirmed by their transformation into (6), (8), (9), and (11) and by alternative synthesis of these compounds.

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