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61045-33-8

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61045-33-8 Usage

General Description

"(2R,3R)-diethyl 1,4-dioxaspiro[4.5]decane-2,3-dicarboxylate" is a chemical compound with the molecular formula C14H22O6. It is a spirocyclic ester that contains a dioxane ring and two carboxylate groups. (2R,3R)-diethyl 1,4-dioxaspiro[4.5]decane-2,3-dicarboxylate has a spiro skeleton with a bridgehead carbon atom, and the diethyl ester groups are attached to the carboxylate moieties. It is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. "(2R,3R)-diethyl 1,4-dioxaspiro[4.5]decane-2,3-dicarboxylate" may also have potential applications in medicinal chemistry and other research fields due to its unique structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 61045-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,4 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61045-33:
(7*6)+(6*1)+(5*0)+(4*4)+(3*5)+(2*3)+(1*3)=88
88 % 10 = 8
So 61045-33-8 is a valid CAS Registry Number.

61045-33-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R)-dioxaspiro[4,5]decane-2,3-dicarboxyldiethylester

1.2 Other means of identification

Product number -
Other names O,O'-cyclohexylidene-Lg-tartaric acid diethyl ester

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:61045-33-8 SDS

61045-33-8Relevant articles and documents

Novel tartrate-derived guanidine-catalyzed highly enantio- and diastereoselective Michael addition of 3-substituted oxindoles to nitroolefins

Zou, Liwei,Bao, Xiaoze,Ma, Yuanyuan,Song, Yuming,Qu, Jingping,Wang, Baomin

supporting information, p. 5760 - 5762 (2014/05/20)

The Michael addition of 3-substituted oxindoles to nitroolefins was catalyzed by a novel tartrate-derived guanidine in high yield with excellent diastereo- and enantioselectivity. This method showed an extraordinarily broad substrate scope in terms of both reaction partners. the Partner Organisations 2014.

Stereoselective total synthesis of synparvolide B and epi-synparvolide A

Srihari,Vijaya Bhasker,Bal Reddy,Yadav

scheme or table, p. 2420 - 2424 (2009/08/07)

Stereoselective total synthesis of synparvolide B and epi-synparvolide A has been achieved following a convergent approach. Noyori asymmetric Transfer Hydrogenation of ketone and Wadsworth-Emmons olefination reaction are the key steps involved.

Synthesis of 1-Deoxy-D-galactohomonojirimycin via Enantiomerically Pure Allenylstannanes

Achmatowicz, Michal,Hegedus, Louis S.

, p. 2229 - 2234 (2007/10/03)

1-Deoxy-D-galactohomonojirimycin was synthesized in seven steps from optically pure allenylstannane 4 and L-lactate-derived aldehyde 5 in 48% overall yield. The key step was the Lewis acid catalyzed reaction of 4 and 5 to give the syn-amino alcohol in exc

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