Cas 608128-59-2,(8S)-1,1-dioxo-2,3,5a,6,7,8-hexahydro-1H-1λ<sup>6</sup>-pyrrolo[1,2-b][1,2]thiazepine-8-carboxylic acid benzyl ester

608128-59-2

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Basic information

Product Name: (8S)-1,1-dioxo-2,3,5a,6,7,8-hexahydro-1H-1λ⁶-pyrrolo[1,2-b][1,2]thiazepine-8-carboxylic acid benzyl ester
Synonyms: (8S)-1,1-dioxo-2,3,5a,6,7,8-hexahydro-1H-1λ⁶-pyrrolo[1,2-b][1,2]thiazepine-8-carboxylic acid benzyl ester
CAS NO:608128-59-2
Molecular Formula:
Molecular Weight: 321.397
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (8S)-1,1-dioxo-2,3,5a,6,7,8-hexahydro-1H-1λ⁶-pyrrolo[1,2-b][1,2]thiazepine-8-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (8S)-1,1-dioxo-2,3,5a,6,7,8-hexahydro-1H-1λ⁶-pyrrolo[1,2-b][1,2]thiazepine-8-carboxylic acid benzyl ester(608128-59-2)
EPA Substance Registry System: (8S)-1,1-dioxo-2,3,5a,6,7,8-hexahydro-1H-1λ⁶-pyrrolo[1,2-b][1,2]thiazepine-8-carboxylic acid benzyl ester(608128-59-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 608128-59-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 608128-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,8,1,2 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 608128-59:
(8*6)+(7*0)+(6*8)+(5*1)+(4*2)+(3*8)+(2*5)+(1*9)=152
152 % 10 = 2
So 608128-59-2 is a valid CAS Registry Number.

608128-59-2Upstream product

608128-59-2Downstream Products

1316754-64-9 (8S)-1,1-dioxo-octahydro-1λ⁶-pyrrolo[1,2-b][1,2]thiazepine-8-carboxylic acid

608128-59-2Relevant academic research and scientific papers

Synthesis of functionally diverse bicyclic sulfonamides as constrained proline analogues and application to the design of potential thrombin inhibitors

Hanessian, Stephen,Sailes, Helen,Therrien, Eric

, p. 7047 - 7056 (2007/10/03)

Bicyclic sulfonamides were synthesized from 4-alkenyl N-alkenylsulfonyl L-prolines using a ring-closure metathesis reaction. Three types of bicyclic sulfonamides varying in the size of the second ring (5,5; 5,6; 5,7) were synthesized. A sulfonamide counte

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