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70713-45-0

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70713-45-0 Usage

Type

Synthetic chemical compound

Class

Protease inhibitor

Primary use

Treatment of HIV/AIDS

Mechanism of action

Inhibits protease enzyme activity

Function

Prevents HIV virus replication

Mode of action

Blocks enzyme to prevent virus multiplication

Combination therapy

Used with other antiretroviral drugs

Effectiveness

Reduces virus level in blood

Benefits

Improves overall health and survival of HIV/AIDS patients

Check Digit Verification of cas no

The CAS Registry Mumber 70713-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,1 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70713-45:
(7*7)+(6*0)+(5*7)+(4*1)+(3*3)+(2*4)+(1*5)=110
110 % 10 = 0
So 70713-45-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H24N2.2ClH/c1-2-13-21-14-16-22(17-15-21)20(18-9-5-3-6-10-18)19-11-7-4-8-12-19;;/h2-12,20H,1,13-17H2;2*1H

70713-45-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzhydryl-4-prop-2-enylpiperazine

1.2 Other means of identification

Product number -
Other names 1-benzhydryl-4-allyl-piperazine

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:70713-45-0 SDS

70713-45-0Downstream Products

70713-45-0Relevant articles and documents

Direct use of allylic alcohols and allylic amines in palladium-catalyzed allylic amination

Jing, Jiangyan,Huo, Xiaohong,Shen, Jiefeng,Fu, Jingke,Meng, Qinghua,Zhang, Wanbin

supporting information, p. 5151 - 5154 (2017/07/12)

Allylic alcohols and allylic amines were directly utilized in a Pd-catalyzed hydrogen-bond-activated allylic amination under mild reaction conditions in the absence of any additives. The cooperative action of a Pd-catalyst and a hydrogen-bonding solvent is most likely responsible for its high reactivity. The catalytic system is compatible with a variety of functional groups and can be used to prepare a wide range of linear allylic amines in good to excellent yields. Furthermore, this methodology can be easily applied to the one-step synthesis of two drugs, cinnarizine and naftifine, on a gram scale.

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