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N-[(7S)-1,2,3-trimethoxy-10-(methylsulfonyl)-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-7-yl]acetamide is a complex organic compound with a molecular formula of C20H23NO7S. It is characterized by a benzo[a]heptalen-7-yl core structure, which is a type of tricyclic aromatic compound. The molecule features three methoxy groups (-OCH3) attached to the benzene ring, a methylsulfonyl group (-S(O)2CH3) at position 10, and a 9-oxo group, indicating the presence of a carbonyl group at position 9. The compound is further modified by an acetamide group (-NHCOCH3) attached to the nitrogen atom. This chemical structure suggests potential applications in pharmaceuticals or as a synthetic intermediate due to its unique arrangement of functional groups, which can influence its reactivity and biological activity.

2826-75-7

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2826-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2826-75-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2826-75:
(6*2)+(5*8)+(4*2)+(3*6)+(2*7)+(1*5)=97
97 % 10 = 7
So 2826-75-7 is a valid CAS Registry Number.

2826-75-7SDS

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 N-[(7S)-1,2,3-trimethoxy-10-methylsulfonyl-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl]acetamide

1.2 Other means of identification

Product number -
Other names N-((S)-10-Methansulfonyl-1,2,3-trimethoxy-9-oxo-5,6,7,9-tetrahydro-benzo[a]heptalen-7-yl)-acetamid

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:2826-75-7 SDS

2826-75-7Upstream product

2826-75-7Downstream Products

2826-75-7Relevant academic research and scientific papers

Quantitative Structure-Activity Relationships of Colchicines against P388 Leukemia in Mice

Quinn, Frank R.,Beisler, John A.

, p. 251 - 256 (2007/10/02)

A quantitative structure-activity relationship (QSAR) was derived for colchicine and 14 analogues acting against P388 lymphocytic leukemia in mice.Twelve additional compounds were synthesized to reinforce and confirm the correlation.The final correlation

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