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9-Methyl-1,5-dioxaspiro[5.5]undecan-3-ol is a complex organic compound with the molecular formula C8H14O3. It is a cyclic ether with a spiro structure, consisting of a seven-membered ring with two oxygen atoms and a methyl group at the 9th position. 9-Methyl-1,5-dioxaspiro[5.5]undecan-3-ol is characterized by its unique molecular structure, which contributes to its specific chemical properties and potential applications. It is typically synthesized through various chemical reactions and can be used in the pharmaceutical industry, as a building block for more complex molecules, or in the synthesis of other organic compounds. Due to its specific structure, it may also have potential applications in materials science or as a reagent in chemical research.

6413-28-1

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6413-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6413-28-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6413-28:
(6*6)+(5*4)+(4*1)+(3*3)+(2*2)+(1*8)=81
81 % 10 = 1
So 6413-28-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O3/c1-8-2-4-10(5-3-8)12-6-9(11)7-13-10/h8-9,11H,2-7H2,1H3

6413-28-1SDS

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 9-methyl-1,5-dioxaspiro[5.5]undecan-3-ol

1.2 Other means of identification

Product number -
Other names 1,9-methyl

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:6413-28-1 SDS

6413-28-1Downstream Products

6413-28-1Relevant articles and documents

Clay catalysed rapid valorization of glycerol towards cyclic acetals and ketals

Pawar, Radheshyam R.,Gosai, Kalpeshgiri A.,Bhatt, Adarsh S.,Kumaresan,Lee, Seung Mok,Bajaj, Hari C.

, p. 83985 - 83996 (2015/10/28)

Biodiesel production usually results in a huge amount of glycerol, raising a critical need to transform it into high value products. The present study highlights that solvent-free, conventional thermal activation, and non-conventional microwave/ultrasonic activation in the liquid phase are able to selectively transform glycerol into cyclic acetals and ketals using an optimised acid activated clay catalyst. Several parameters for the acid activation of bentonite clay were optimized under mild reaction conditions with a high concentration of clay (6%) and varying the acid concentration in the range of 6 to 15 N. The acid-activated clay samples were characterized by XRD, FT-IR, BET, and XRF analysis. The active sites of the catalyst were examined by volumetric titration and confirmed by pyridine adsorbed FT-IR and advanced NH3-TPD analyses. The activation performed at relatively mild conditions, i.e.; 6 N H2SO4 and 6% w/v clay, reproducibly resulted in an improved surface area (180 m2 g-1) and surface acidity (23 mg KOH g-1), with superior quantitative Br?nsted and Lewis acidic sites. Moreover, the eco-friendly process involving a catalyst, microwave, or ultra-sonication were successfully utilized to achieve a commercially valuable hyacinth fragrance, in addition to furan-based fuel additive precursors exhibiting a high conversion of glycerol and excellent selectivity within much less activation time (2 min).

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