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Benzenamine, 4-(1-naphthalenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76180-77-3

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76180-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76180-77-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,8 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76180-77:
(7*7)+(6*6)+(5*1)+(4*8)+(3*0)+(2*7)+(1*7)=143
143 % 10 = 3
So 76180-77-3 is a valid CAS Registry Number.

76180-77-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-naphthalen-1-ylsulfanylaniline

1.2 Other means of identification

Product number -
Other names -

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:76180-77-3 SDS

76180-77-3Relevant academic research and scientific papers

Crystallographic and SAR analyses reveal the high requirements needed to selectively and potently inhibit SIRT2 deacetylase and decanoylase

Yang, Ling-Ling,Xu, Wei,Yan, Jie,Su, Hui-Lin,Yuan, Chen,Li, Chao,Zhang, Xing,Yu, Zhu-Jun,Yan, Yu-Hang,Yu, Yamei,Chen, Qiang,Wang, Zhouyu,Li, Lin,Qian, Shan,Li, Guo-Bo

supporting information, p. 164 - 168 (2019/01/30)

A high-quality X-ray crystal structure reveals the mechanism of compound 1a inhibiting SIRT2 deacetylase and decanoylase. Structure-activity relationship (SAR) analysis of the synthesized derivatives of 1a reveals the high requirements needed for selectiv

CsOH·H2O-promoted synthesis of aryl sulfides via direct coupling of aryl halides and thiols

Varala, Ravi,Ramu,Mujahid Alam,Adapa, Srinivas R.

, p. 1614 - 1615 (2007/10/03)

We report here our observation that, using appropriate reaction conditions, CsOH·H2O-promoted coupling of aryl halides with thiols can be performed in moderate to good yields without a transition metal catalyst. Copyright

INHIBITORS OF AMYLOID BETA-PROTEIN PRODUCTION

-

, (2008/06/13)

A method of protecting a warm-blooded mammal from the progression of Alzheimer"s disease, which comprises administering an effective amount of a compound of general formula.

CHEMICAL COMPOUNDS AS INHIBITORS OF AMYLOID BETA PROTEIN PRODUCTION

-

, (2008/06/13)

A compound of the formula I in which Z is O or S; R11 is a halogen atom; R12 is a halogen atom or a trifluoromethyl group; and X is S, SO, SO2, O or NH; R4 is naphthyl, quinolinyl, benzimidazolyl, pyridyl, pyradazinyl, benzoxazolyl or benzothiazolyl, unsubstituted or substituted by one or two substituents selected from a halogen atom, (1-4C)alkyl, (1-4C)alkoxy, nitro, (1-4C)alkoxycarbonyl, halo(1-4C)alkyl, and phenyl; or a pharmaceutically acceptable salt thereof. The compounds are useful as inhibitors of amyloid beta-protein production.

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