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88122-95-6

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88122-95-6 Usage

Uses

3-Hydroxy-4-sulfobenzoic Acid, is used for the synthesis of arginine vasopressin V2 receptor antagonist SR-121463.

Check Digit Verification of cas no

The CAS Registry Mumber 88122-95-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,2 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88122-95:
(7*8)+(6*8)+(5*1)+(4*2)+(3*2)+(2*9)+(1*5)=146
146 % 10 = 6
So 88122-95-6 is a valid CAS Registry Number.

88122-95-6SDS

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 3-hydroxy-4-sulfobenzoic acid

1.2 Other means of identification

Product number -
Other names 2-hydroxyl-4-carboxylbenzenesulfonic 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:88122-95-6 SDS

88122-95-6Relevant articles and documents

Total synthesis of SR 121463 A, a highly potent and selective vasopressin V2 receptor antagonist

Venkatesan,Davis,Altas,Snyder,Liotta

, p. 3653 - 3661 (2007/10/03)

SR 121463 A, 1, is a promising nonpeptide prototype for potent and selective antagonism of the vasopressin V2 receptor subtype and, thus, a candidate for control of the clinically debilitating condition of hyponatremia and its associated syndromes. In the present work, we present a novel and stereoselective synthesis that stems from the preparation of three key intermediates: the substituted benzenesulfonyl chloride 2, the N-protected oxindole 3, and protected dibromide 4. The synthesis of 1 has been achieved in good overall yield, each step proceeding in greater than 80% yield. In addition, intermediate 2 and the syn isomer of 1 were prepared with complete control of stereochemistry. The latter reduction appears to proceed by lithium cation mediated chelation control. Molecular mechanics calculations with the MM3* and MMFF force fields underscore geometric and energetic aspects of the reaction.

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