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6629-36-3

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6629-36-3 Usage

Molecular structure

2-(3,4-dimethylphenyl)-2-oxoethyl (1,3-dioxooctahydro-4,6-ethenocyclopropa[f]isoindol-2(1H)-yl)acetate has a complex chemical structure with various functional groups including ester, ketone, and aromatic rings.

Type of compound

It is a synthetic organic compound.

Usage

Commonly used in the field of organic chemistry for research purposes and potentially in drug development.

Unique properties

Known for its unique molecular structure which may lead to potential applications in various fields.

Specialized handling

Requires specialized handling and expertise due to its complex nature.

Potentially hazardous

Possesses potentially hazardous properties that necessitate careful handling and precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 6629-36-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6629-36:
(6*6)+(5*6)+(4*2)+(3*9)+(2*3)+(1*6)=113
113 % 10 = 3
So 6629-36-3 is a valid CAS Registry Number.

6629-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-(benzenesulfonyl)-N-benzylcarbamate

1.2 Other means of identification

Product number -
Other names N-Benzyl-N-benzolsulfonyl-carbaminsaeure-benzylester

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:6629-36-3 SDS

6629-36-3Downstream Products

6629-36-3Relevant articles and documents

METHOD FOR THE ORGANOMETALLIC PRODUCTION OF ORGANIC INTERMEDIATE PRODUCTS COMPRISING CARBON-HETEROATOM BONDS ACHIEVED BY THE DEPROTONATION OF HETEROATOMS

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Page/Page column 14, (2008/06/13)

The invention relates to a method for binding heteroatom-carbon bonds. According to said method, a lithium compound (II) is first generated by reacting aliphatic or aromatic halogen compounds (I) with lithium metal, said compound is then used for the deprotonation of the compounds (III) or (V). The lithium salts of formulas (IV) or (VI) obtained by said deprotonation are subsequently reacted with suitable carbon electrophiles (equation I), said process binding the heteroatom-carbon bond and forming the products (VIII) or (VIII), (equation I).

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