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1,3-Cyclopentanedicarboxylic acid, 1,2-dimethyl-2-(phenylmethyl)-, dimethyl ester, (1R,2S,3S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

750644-70-3

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750644-70-3 Usage

Class of Compound

ACE inhibitors

Medical Use

Treatment of high blood pressure and heart failure

Mechanism of Action

Relaxing blood vessels to improve blood flow and reduce the workload on the heart

Administration

Oral (tablets and capsules)

Combination Therapy

Often used in combination with other medications to manage cardiovascular conditions

Benefits

Effective in reducing the risk of stroke, heart attack, and kidney problems in patients with diabetes

Side Effects

Dizziness, cough, and low blood pressure

Precautions

Use as directed by a healthcare professional and be aware of potential side effects

Check Digit Verification of cas no

The CAS Registry Mumber 750644-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,0,6,4 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 750644-70:
(8*7)+(7*5)+(6*0)+(5*6)+(4*4)+(3*4)+(2*7)+(1*0)=163
163 % 10 = 3
So 750644-70-3 is a valid CAS Registry Number.

750644-70-3Upstream product

750644-70-3Relevant academic research and scientific papers

Toward the development of a general chiral auxiliary 10: Enhancement of diastereoselectivity in Diels-Alder reactions of imides derived from a new bicyclic lactam chiral controller molecule

Boeckman Jr., Robert K.,Reeder, Lisa M.

, p. 1399 - 1403 (2004)

Based upon X-ray structural information derived from a series of camphor-derived bicyclic lactam chiral controller molecules, a new auxiliary has been designed which affords superior diastereoselectivity (>95:5) in Diels-Alder reactions with common dienes but of opposite π-facial selectivity than previously observed with this class of chiral controller. A rationale for the selectivity based on subtle structural changes in the chiral controller is discussed.

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