Basic information

Product Name: L-Alaninamide, N-[(phenylmethoxy)carbonyl]-L-tryptophyl-
Synonyms:
CAS NO:105099-86-3
Molecular Formula: C22H24N4O4
Molecular Weight: 408.457
EINECS: N/A
Product Categories: N/A
Mol File: 105099-86-3.mol

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: L-Alaninamide, N-[(phenylmethoxy)carbonyl]-L-tryptophyl-(CAS DataBase Reference)
NIST Chemistry Reference: L-Alaninamide, N-[(phenylmethoxy)carbonyl]-L-tryptophyl-(105099-86-3)
EPA Substance Registry System: L-Alaninamide, N-[(phenylmethoxy)carbonyl]-L-tryptophyl-(105099-86-3)

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: 105099-86-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 105099-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,0,9 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 105099-86:
(8*1)+(7*0)+(6*5)+(5*0)+(4*9)+(3*9)+(2*8)+(1*6)=123
123 % 10 = 3
So 105099-86-3 is a valid CAS Registry Number.

105099-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	Cbz-L-Trp-L-Ala-NH2

1.2 Other means of identification

Product number	-
Other names	benzyl N-[(1S)-2-[(1S)-2-amino-1-methyl-2-oxoethyl]-amino-1-(1H-indol-2-ylmethyl)-2-oxoethyl]carbamate

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:105099-86-3 SDS

105099-86-3Upstream product

886981-41-5 benzyl N-{(S)-1-[(S)-2-benzotriazol-1-yl-1-methyl-2-oxoethylcarbamoyl]-2-(1H-indol-3-yl)-ethyl}carbamate

105099-86-3Downstream Products

105099-86-3Relevant academic research and scientific papers

Convenient synthesis of C-terminal di- and tri-peptide amides from N-protected dipeptidoylbenzotriazoles

Celik, Ilhami,Abdel-Fattah, Ashraf A.A.

, p. 4923 - 4929 (2009)

N-Protected dipeptidoylbenzotriazoles react with aqueous ammonia to give dipeptide primary amides (77-98%) and with N-unprotected α-amino amides to afford tripeptide primary amides (82-86%).

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