Cas 638165-82-9,2-(2S)-[(6S)-(6-benzyloxymethyl-1,1-dioxo-2,3,6,7-tetrahydro-1,2,7-thiadiazepin-2-yl)]-3-methyl-butyric acid methyl ester

638165-82-9

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Basic information

Product Name: 2-(2S)-[(6S)-(6-benzyloxymethyl-1,1-dioxo-2,3,6,7-tetrahydro-1,2,7-thiadiazepin-2-yl)]-3-methyl-butyric acid methyl ester
Synonyms: 2-(2S)-[(6S)-(6-benzyloxymethyl-1,1-dioxo-2,3,6,7-tetrahydro-1,2,7-thiadiazepin-2-yl)]-3-methyl-butyric acid methyl ester
CAS NO:638165-82-9
Molecular Formula:
Molecular Weight: 382.481
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: 2-(2S)-[(6S)-(6-benzyloxymethyl-1,1-dioxo-2,3,6,7-tetrahydro-1,2,7-thiadiazepin-2-yl)]-3-methyl-butyric acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2S)-[(6S)-(6-benzyloxymethyl-1,1-dioxo-2,3,6,7-tetrahydro-1,2,7-thiadiazepin-2-yl)]-3-methyl-butyric acid methyl ester(638165-82-9)
EPA Substance Registry System: 2-(2S)-[(6S)-(6-benzyloxymethyl-1,1-dioxo-2,3,6,7-tetrahydro-1,2,7-thiadiazepin-2-yl)]-3-methyl-butyric acid methyl ester(638165-82-9)

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: 638165-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 638165-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,8,1,6 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 638165-82:
(8*6)+(7*3)+(6*8)+(5*1)+(4*6)+(3*5)+(2*8)+(1*2)=179
179 % 10 = 9
So 638165-82-9 is a valid CAS Registry Number.

638165-82-9Upstream product

638165-82-9Downstream Products

638165-83-0 2-(2S)-[(6S)-(7-benzyl-6-benzyloxymethyl-1,1-dioxo-2,3,6,7-tetrahydro-1,2,7-thiadiazepin-2-yl)]-3-methyl-butyric acid methyl ester

638165-82-9Relevant academic research and scientific papers

New strategies to symmetric and unsymmetric cyclic sulfamide analogs of DMP 323: A 'sulfur linchpin'/RCM approach

Jun, Jung Ho,Dougherty, Joseph M.,Jiménez, María Del Sol,Hanson, Paul R.

, p. 8901 - 8912 (2007/10/03)

The synthesis of 7-membered cyclic sulfamides utilizing the RCM reaction is described herein. Two major synthetic strategies that expand the scope and utility of our previously reported sulfamide and sulfamoyl carbamate chemistry are employed. Both Mitsun

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