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N-Benzhydryl-succinamic acid, also known as N-benzylsuccinamic acid, is a chemical compound with the molecular formula C11H13NO3. It is a white crystalline solid that is soluble in water and various organic solvents. N-BENZHYDRYL-SUCCINAMIC ACID is derived from the combination of benzhydryl (a diphenylmethyl group) and succinamic acid (a derivative of succinic acid with an amino group). N-Benzhydryl-succinamic acid is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Its unique structure allows for the formation of diverse products through chemical reactions, making it a valuable building block in the field of organic chemistry.

6622-07-7

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6622-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6622-07-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6622-07:
(6*6)+(5*6)+(4*2)+(3*2)+(2*0)+(1*7)=87
87 % 10 = 7
So 6622-07-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H17NO3/c19-15(11-12-16(20)21)18-17(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-10,17H,11-12H2,(H,18,19)(H,20,21)

6622-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(benzhydrylamino)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names N-Benzhydryl-succinamic acid

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:6622-07-7 SDS

6622-07-7Relevant academic research and scientific papers

Triggering a [2]Rotaxane Molecular Shuttle by a Photochemical Bond-Cleavage Strategy

Gao, Chuan,Luan, Zhou-Lin,Zhang, Qi,Yang, Shun,Rao, Si-Jia,Qu, Da-Hui,Tian, He

, p. 1618 - 1621 (2017)

The successful triggering of ring-shuttling motion between two stations in a [2]rotaxane is demonstrated by employing a photochemical bond-cleavage strategy. A photolabile bulk barrier is covalently introduced into two identical stations of the thread to

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