Cas 150372-62-6,[2-((S)-2-Benzyloxycarbonylamino-3-methyl-butyrylamino)-2-methyl-propionylamino]-acetic acid methyl ester

150372-62-6

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Basic information

Product Name: [2-((S)-2-Benzyloxycarbonylamino-3-methyl-butyrylamino)-2-methyl-propionylamino]-acetic acid methyl ester
Synonyms:
CAS NO:150372-62-6
Molecular Formula:
Molecular Weight: 407.467
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-((S)-2-Benzyloxycarbonylamino-3-methyl-butyrylamino)-2-methyl-propionylamino]-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [2-((S)-2-Benzyloxycarbonylamino-3-methyl-butyrylamino)-2-methyl-propionylamino]-acetic acid methyl ester(150372-62-6)
EPA Substance Registry System: [2-((S)-2-Benzyloxycarbonylamino-3-methyl-butyrylamino)-2-methyl-propionylamino]-acetic acid methyl ester(150372-62-6)

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: 150372-62-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 150372-62-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,3,7 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 150372-62:
(8*1)+(7*5)+(6*0)+(5*3)+(4*7)+(3*2)+(2*6)+(1*2)=106
106 % 10 = 6
So 150372-62-6 is a valid CAS Registry Number.

150372-62-6Upstream product

150372-62-6Downstream Products

150372-62-6Relevant academic research and scientific papers

Efficient synthesis of alamethicin F-30 using a chloro imidazolidium coupling reagent, CIP

Akaji, Kenichi,Tamai, Yasunori,Kiso, Yoshiaki

, p. 9341 - 9344 (1995)

Alamethicin F-30 has been synthesized in solution using a CIP-additive as a coupling agent and TFA as a final deprotecting reagent. All couplings including those between sterically hindered α,α-dimethyl amino acid were successfully achieved by a 60 min re

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