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99661-07-1

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99661-07-1 Usage

Chemical Class

Heterocyclic compounds, specifically benzothiophenes

Structure

Contains a thiophene ring fused to a benzene ring

Common Uses

Organic synthesis
Pharmaceutical research

Biological Activities

Anti-inflammatory properties
Antioxidant properties

Chemical Modification

The presence of a bromine atom makes it suitable for further chemical modifications

Potential Applications

Medicine
Agriculture
Materials science

Check Digit Verification of cas no

The CAS Registry Mumber 99661-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,6,6 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99661-07:
(7*9)+(6*9)+(5*6)+(4*6)+(3*1)+(2*0)+(1*7)=181
181 % 10 = 1
So 99661-07-1 is a valid CAS Registry Number.

99661-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-bromo-1-benzothiophen-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names acetyl-2 bromo-3 benzo<b>thiophene

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:99661-07-1 SDS

99661-07-1Relevant articles and documents

HETEROCYCLIC COMPOUNDS AND THEIR USES

-

Page/Page column 53, (2011/10/13)

Substituted bicyclic heteroaryls and compositions containing them, for the treatment of general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, including but not restricted to autoimmune diseases such as systemic lupus erythematosis (SLE), myestenia gravis, rheumatoid arthritis, acute disseminated encephalomyelitis, idiopathic thrombocytopenic purpura, multiples sclerosis, Sjoegren's syndrome and autoimmune hemolytic anemia, allergic conditions including all forms of hypersensitivity, The present invention also enables methods for treating cancers that are mediated, dependent on or associated with p110δ activity, including but not restricted to leukemias, such as Acute Myeloid leukaemia (AML) Myelo-dysplastic syndrome (MDS) myelo-proliferative diseases (MPD) Chronic Myeloid Leukemia (CML) T-cell Acute Lymphoblastic leukaemia (T-ALL) B-cell Acute Lymphoblastic leukaemia (B-ALL) Non Hodgkins Lymphoma (NHL) B-cell lymphoma and solid tumors, such as breast cancer.

Preparation of benzene, furan, and thiophene analogs of duocarmycin SA employing a newly-devised phenol-forming reaction

Muratake,Hayakawa,Natsume

, p. 1558 - 1566 (2007/10/03)

Five A-ring analogs of duocarmycin SA 9a - e were synthesized in racemic form modifying our second synthetic route toward duocarmycin SA. The problem encountered at the crucial phenol forming step to secure 17a, b from 16a, b under the conventionally used

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