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89291-75-8

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  • (3AR,6AR)-6-(BENZYLOXYMETHYL)-2,2-DIMETHYL-3AH-CYCLOPENTA[D][1,3]DIOXOL-4(6AH)-ONE

    Cas No: 89291-75-8

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89291-75-8 Usage

Description

(3aR,6aR)-6-(benzyloxymethyl)-2,2-dimethyl-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-one, also known as Benzyloxymethyl 4-oxo-6,6-dimethyl-1,2,3,3a,6,6a-hexahydrofuro[3,4-d][1,3]dioxol-3a-yl ether, is a synthetic organic compound with the molecular formula C15H20O4. It is commonly used in the field of organic chemistry for various purposes, such as the development of new pharmaceuticals, agrochemicals, or materials. Its specific properties and potential applications are subject to further research and development in the scientific community.

Uses

Used in Pharmaceutical Industry:
(3aR,6aR)-6-(benzyloxymethyl)-2,2-dimethyl-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-one is used as a building block or intermediate in the synthesis of new pharmaceuticals for various therapeutic applications. Its unique structure and functional groups make it a promising candidate for the development of innovative drugs.
Used in Agrochemical Industry:
(3aR,6aR)-6-(benzyloxymethyl)-2,2-dimethyl-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-one is used as a key component in the development of new agrochemicals, such as pesticides or herbicides, to improve crop protection and yield.
Used in Materials Science:
(3aR,6aR)-6-(benzyloxymethyl)-2,2-dimethyl-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-one is used as a precursor or additive in the synthesis of new materials with specific properties, such as polymers, coatings, or composites, for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 89291-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,9 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89291-75:
(7*8)+(6*9)+(5*2)+(4*9)+(3*1)+(2*7)+(1*5)=178
178 % 10 = 8
So 89291-75-8 is a valid CAS Registry Number.

89291-75-8SDS

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 (3aR,6aR)-2,2-dimethyl-6-(phenylmethoxymethyl)-3a,6a-dihydrocyclopenta[d][1,3]dioxol-4-one

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:89291-75-8 SDS

89291-75-8Relevant articles and documents

Fluorocyclopentenyl-cytosine with broad spectrum and potent antitumor activity

Choi, Won Jun,Chung, Hwa-Jin,Chandra, Girish,Alexander, Varughese,Zhao, Long Xuan,Lee, Hyuk Woo,Nayak, Akshata,Majik, Mahesh S.,Kim, Hea Ok,Kim, Jin-Hee,Lee, Young B.,Ahn, Chang H.,Lee, Sang Kook,Jeong, Lak Shin

, p. 4521 - 4525 (2012/08/13)

On the basis of the potent biological activity of cyclopentenyl- pyrimidines, fluorocyclopentenyl-pyrimidines were designed and synthesized from d-ribose. Among these, the cytosine derivative 5a showed highly potent antigrowth effects in a broad range of

Preparative Synthesis of the Key Intermediate, (4R,5R)-3-Benzyloxymethyl-4,5-isopropylidenedioxycyclopent-2-enone for Carbocyclic Nucleosides

Moon, Hyung Ryong,Choi, Won Jun,Kim, Hea Ok,Jeong, Lak Shin

, p. 506 - 507 (2007/10/03)

(4R,5R)-3-Benzyloxymethyl-4,5-isopropylidenedioxycyclopent-2-enone (1), a versatile intermediate for the synthesis of carbocyclic nucleosides was synthesized from D-ribose in 10 steps and 26 percent overall yield.

Synthesis using ring closure metathesis and effect on nucleoside transport of a (N)-methanocarba S-(4-nitrobenzyl)thioinosine derivative

Lee, Kyeong,Cass, Carol,Jacobson, Kenneth A.

, p. 597 - 599 (2007/10/03)

(Matrix presented) A new synthetic route to ring-constrained (N)-methanocarba nucleosides and nucleotides is presented. Ring closure of a diene intermediate usina Grubbs catalyst provides a new avenue for the preparation of the cyclopentenone derivative 6

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