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929693-35-6

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929693-35-6 Usage

General Description

(1S,3S,6R)-N,N-dimethyl-7-oxabicyclo[4.1.0]heptane-3-carboxamide is a chemical compound with a complex structure. It is a bicyclic compound containing a carbonyl group and an amide functional group. The (1S,3S,6R) stereochemistry indicates the specific arrangement of atoms around the chiral centers within the molecule. The N,N-dimethyl moiety refers to two methyl groups attached to a nitrogen atom. (1S,3S,6R)-N,N-dimethyl-7-oxabicyclo[4.1.0]heptane-3-carboxamide may have potential pharmacological or biological activities due to its complex structure and stereochemistry, and it could be used as a building block in organic synthesis or drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 929693-35-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,6,9 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 929693-35:
(8*9)+(7*2)+(6*9)+(5*6)+(4*9)+(3*3)+(2*3)+(1*5)=226
226 % 10 = 6
So 929693-35-6 is a valid CAS Registry Number.

929693-35-6Relevant articles and documents

Preparation method of edoxaban

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, (2019/07/08)

The invention relates to a new preparation route and a new method for a p-toluenesulfonic acid edoxaban hydrate and intermediates thereof. The new method comprises the steps that a high-reactivity compound 109A4x is prepared; a compound 109C6x is prepared by using a new synthesizing method; new compounds 109E8-01, 109E9x and 109T7-01 are prepared; the p-toluenesulfonic acid edoxaban hydrate is prepared by using the intermediates. By using the new method and the new route, the reaction step of copious cooling is omitted, and dangerous elemental sulfur, high-risk n-butyllithium and high-risk azides are prevented from being used. In a word, by means of the method, the p-toluenesulfonic acid edoxaban hydrate and the key intermediates thereof are more easily and safely prepared at a lower coston an industrialization scale.

Processes for the Preparation of Edoxaban and Intermediates Thereof

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, (2018/07/15)

The present invention provides processes for the preparation of Edoxaban (1) and salts thereof, as well as intermediates thereof. In particular, intermediate compounds and/or salts of the Formulae (3), (4), (6-A), (7-A), (8-A), (9-A) and (10-AS) are provided.

A method for producing an optically active Dimamine deriv.

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, (2016/10/09)

The problem to be solved is to provide a method for efficiently producing compounds (1) and (1a) that are important intermediate compounds in the production of FXa inhibitors (X) and (X-a). The solutions thereto are a method for producing a compound represented by the formula (8d) using a stereoselective intramolecular cyclization reaction, and a method for producing a compound (If) or a salt thereof, or a hydrate thereof, which is characterized by desulfonylation of the compound (8d). In each formula, R 4a represents a C1-C6 alkyl group, a benzyl group, etc.

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