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NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine

NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine structure

CAS No.: 141743-13-7

Chemical Name:: NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine

Synonyms: N-FMoc-N-benzyl-glycine;Fmoc-N-benzylglycine≥ 99% (HPLC);NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine;N-α-(9-Fluorenylmethoxycarbonyl)-N-α-benzyl-glycine;Glycine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-(phenylmethyl)-;2-[benzyl({[(9H-fluoren-9-yl)methoxy]carbonyl})amino]acetic acid;2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(benzyl)amino)acetic acid

CBNumber:: CB61486296

Molecular Formula:: C24H21NO4

Molecular Weight:: 387.43

MDL Number:: MFCD04112686

MOL File:: 141743-13-7.mol

MSDS File:: SDS

Last updated:2022-08-26 12:27:30

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NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine Properties

Boiling point	604.0±44.0 °C(Predicted)
Density	1.285±0.06 g/cm3(Predicted)
storage temp.	Sealed in dry,2-8°C
pka	3.89±0.10(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)	GHS07
Signal word	Warning
Hazard statements	H315-H319-H335
Precautionary statements	P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501
HS Code	29225090

NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine price More Price(14)

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
TRC	F621065	Fmoc-N-benzylglycine	141743-13-7	5g	$745	2021-12-16	Buy
Activate Scientific	AS85305	N-Fmoc-N-benzyl-glycine 95+%	141743-13-7	1g	$115	2021-12-16	Buy
Iris Biotech GmbH	FAA1450	Fmoc,Bzl-Gly-OH	141743-13-7	5G	$270	2021-12-16	Buy
AK Scientific	V3127	Fmoc-bzl-gly-oh	141743-13-7	5g	$279	2021-12-16	Buy
Activate Scientific	AS85305	N-Fmoc-N-benzyl-glycine 95+%	141743-13-7	5G	$347	2021-12-16	Buy

Product number	Packaging	Price	Buy
F621065	5g	$745	Buy
AS85305	1g	$115	Buy
FAA1450	5G	$270	Buy
V3127	5g	$279	Buy
AS85305	5G	$347	Buy

NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine Chemical Properties,Uses,Production

Chemical Properties

Colorless to white crystals powder

Uses

Fmoc-?N-?benzylglycine is a reactant used in the solid phase synthesis of peptides. It was used in the synthesis of endomorphin 1 and 2 peptoid-peptide hybrids. Fmoc-?N-?benzylglycine was also used in the synthesis of human neuropeptide-S analogs modified in position 2.

NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine Preparation Products And Raw materials

Raw materials

Preparation Products

NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine Suppliers

Global( 38)Suppliers

Supplier	Tel	Email	Country	ProdList	Advantage
Nanjing Dolon Biotechnology Co.,Ltd.	18905173768	sales@dolonchem.com	CHINA	2972	58
GL Biochem(Binhai) Ltd.	+86-021-61263370 +8615301650015	wuqiuyan@glschina.com	China	2975	58
BOC Sciences	+16314854226	inquiry@bocsci.com	United States	19743	58
Nextpeptide Inc	+86-0571-81612335 +8613336028439	sales@nextpeptide.com	China	19915	58
LEAP CHEM CO., LTD.	+86-852-30606658	market18@leapchem.com	China	24738	58
Aladdin Scientific	+1-833-552-7181	sales@aladdinsci.com	United States	52927	58
DONBOO AMINO ACID COMPANY	+8613063595538	donboo@donboo.com	China	9365	58
J & K SCIENTIFIC LTD.	010-82848833 400-666-7788	jkinfo@jkchemical.com	China	94838	76
Shanghai Hanhong Scientific Co.,Ltd.	021-54306202 13764082696;	info@hanhongsci.com	China	42982	64
Chemsky (shanghai) International Co.,Ltd	021-50135380	shchemsky@sina.com	China	15421	60

Supplier	Advantage
Nanjing Dolon Biotechnology Co.,Ltd.	58
GL Biochem(Binhai) Ltd.	58
BOC Sciences	58
Nextpeptide Inc	58
LEAP CHEM CO., LTD.	58
Aladdin Scientific	58
DONBOO AMINO ACID COMPANY	58
J & K SCIENTIFIC LTD.	76
Shanghai Hanhong Scientific Co.,Ltd.	64
Chemsky (shanghai) International Co.,Ltd	60

141743-13-7(NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine)Related Search:

N-Fmoc-N-(3-methyl-3-acetylamido)propyl)-Glycine N-(((9H-fluoren-9-yl)methoxy)carbonyl)-N-(4-(tert-butoxy)-4-oxobutyl)glycine N-Fmoc-N-(3-acetamidopropyl)glycine N-Fmoc-N-(3-methylsulfonamido)propyl)-Glycine N-Fmoc-N-(cyclohexylmethyl)-glycine

Pentanoic acid, 5-[(carboxymethyl)[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, 1-(1,1-dimethylethyl) ester Hexanoic acid, 6-[(carboxymethyl)[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, 1-(1,1-dimethylethyl) ester Glycine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-(3-phenylpropyl)- N-Fmoc-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid FMOC-TIC-OH

FMOC-7-HYDROXY-(R)-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine FMOC-(FMOCHMB)ALA-OH FMOC-(4S,2RS)-2-PHENYLTHIAZOLIDINE-4-CARBOXYLIC ACID FMOC-(FMOCHMB)LEU-OH

FMOC-7-HYDROXY-(S)-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID FMOC-(FMOCHMB)PHE-OH FMOC-N-ALPHA-(4-AMINOBENZOYL)-L-GLUTAMIC ACID

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NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine N-FMoc-N-benzyl-glycine 2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(benzyl)amino)acetic acid Fmoc-N-benzylglycine≥ 99% (HPLC) N-α-(9-Fluorenylmethoxycarbonyl)-N-α-benzyl-glycine Glycine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-(phenylmethyl)- 2-[benzyl({[(9H-fluoren-9-yl)methoxy]carbonyl})amino]acetic acid 141743-13-7