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Cyclohexanone, 6-(3,4-dihydro-1H-2-benzopyran-1-yl)-2,2-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100008-36-4

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100008-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100008-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,0 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100008-36:
(8*1)+(7*0)+(6*0)+(5*0)+(4*0)+(3*8)+(2*3)+(1*6)=44
44 % 10 = 4
So 100008-36-4 is a valid CAS Registry Number.

100008-36-4SDS

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 6-(3,4-dihydro-1H-isochromen-1-yl)-2,2-dimethylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names Cyclohexanone,6-(3,4-dihydro-1H-2-benzopyran-1-yl)-2,2-dimethyl

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:100008-36-4 SDS

100008-36-4Relevant academic research and scientific papers

Synthesis of Carbocyclic Spiro Compounds from Isochroman Derivatives via Intramolecular Aldol Reaction

Hashigaki, Kuniko,Yoshioka, Sabroh,Yamato, Masatoshi

, p. 1004 - 1007 (1986)

Condensation of 1-ethoxyisochromans with cyclohexanones, 1-indanone, or 1-tetralone in the presence of boron trifluoride etherate affords α-(isochroman-1-yl)-cyclic ketones.Reductive ring cleavage of the isochromanyl moiety followed by Jones oxidation yie

TRANSFORMATION OF (ISOCHROMAN-1-YL)METHYLENEKETONES TO NAPHTHALENE DERIVATIVES

Yamato, Masatoshi,Hashigaki, Kuniko,Yoshioka, Sabroh,Takeuchi, Yasuo

, p. 1741 - 1750 (2007/10/02)

Treatment of (isochroman-1-yl)methylketones (2c-h) with potassium tert-butoxide gave different naphthalene derivatives (5-14) via novel ring transformation, depending on the presence or absence and the nature of the substituents adjacent to the carbonyl group in 2.

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