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27219-07-4

27219-07-4 structure
27219-07-4 structure
  • Name: Boc-NH-C4-acid
  • Chemical Name: 5-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid
  • CAS Number: 27219-07-4
  • Molecular Formula: C10H19NO4
  • Molecular Weight: 217.262
  • Catalog: Biochemical Amino acids and their derivatives BOC-amino acid
  • Create Date: 2018-07-05 14:31:34
  • Modify Date: 2026-07-16 22:13:05
  • Boc-NH-C4-acid is a PROTAC linker, which belongs to a Alkyl/ether linker. Boc-NH-C4-acid can be used in the synthesis of the compound PROTAC1, and specifically degrades EED, EZH2, and SUZ12 in the PRC2 Complex.

Name 5-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid
Synonyms 5-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)pentanoic acid
N-T-BUTOXYCBONYL-5-AMINOPENTANOIC ACID
MFCD00076903
5-[(tert-Butoxycarbonyl)amino]valeric Acid
BOC-NH-(CH2)4-COOH
Boc-5-Ava-OH
5-(tert-Butoxycbonylamino)pentanoic Acid N-Boc-5-aminovaleric Acid N-Boc-5-aminopentanoic Acid
N-(tert-Butoxycarbonyl)-5-aminovaleric Acid
Boc-2-amino-5-phenylpentanoic acid DCHA
5-(TERT-BUTOXYCBONYLAMINO)VALERIC ACID
Hexanedioic acid, 2-amino-, 1-(1,1-dimethylethyl) ester
N-(tert-Butoxycbonyl)-5-aminovaleric Acid >
N-(tert-Butoxycbonyl)-5-aMinovaleric Acid
BOC-5-AMINOVALERIC ACID
RECHEM EM WB 0073
BOC-5-AMINOPENTANOIC ACID
Boc-5-aminovaleric acid (HPLC)
5-(tert-Butoxycarbonylamino)pentanoic Acid
N-Boc-5-aminovaleric Acid
PROTAC Linkers,Inhibitor,protac,Boc NH C4 acid,inhibit,BocNHC4acid,Boc-NH-C-4-acid,linker
5-Boc-amino-pentanoic acid
5-(tert-Butoxycarbonylamino)valeric Acid
N-BOC-5-AMINOVALERIC ACID
N-(tert-Butoxycbonyl)-5-aminopentanoic Acid
5-(N-t-butoxycarbonylamino)valeric acid
5-[(2-methylpropan-2-yl)oxycbonylamino]pentanoic acid
Boc-d-aMinovaleric acid
PENTANOIC ACID, 5-[[(1,1-DIMETHYLETHOXY)carbonyl]AMINO]
5-(BOC-AMINO)PENTANOIC ACID
5-(N-t-butyloxycarbonylamino)-pentanoic acid
(Tert-Butoxy)carbonyl 5-Ava-OH
5-[(2-methylpropan-2-yl)oxycbonylamino]pentanoicaci
Boc-5-aminopentanoic acid
5-(TERT-BUTOXYCBONYLAMINO)PENTANOIC ACID
N-BOC-5-AMINOPENTANOIC ACID
5-[(tert-Butoxycarbonyl)amino]pentanoic acid
5-(N-t-butoxycarbonylamino)pentanoic acid
5-(BOC-AMINO)VALERIC ACID
5-[(tert-Butyloxycbonyl)amino]pentanoic acid
5-[[(1,1-Dimethylethoxy)carbonyl]amino]-pentanoic acid
5-(Boc-amino)pentanoic acid, 5-(Boc-amino)valeric acid
5-[[(1,1-Dimethylethoxy)carbonyl]amino]pentanoic acid
BOC-DELTA-AMINOVALERIC ACID
Boc-5-AMinovaleric acid Boc-5-AMinovaleric acid
5-(Boc-amino)valeric acid
N-(tert-Butoxycbonyl)-5-aminop
5-(N-BOC-Amino)pentanoic acid
2-Methyl-2-propanyl 6-hydroxy-6-oxonorleucinate
5-[[(1,1-Dimethylethyl)oxy]carbonyl]aminopentanoic acid
BOC-APE(5)-OH
5-(Boc-amino)pentanoic Acid
N-DELTA-T-BUTOXYCBONYL-DELTA-AMINOVALERIC ACID
5-(N-Boc-amino)valeric acid
Boc-5-aminopentanoic acid //BP
tert-butyl 1-phenyl-2,9,12,15-tetraoxahtadecan-17-oate
N-Boc-5-aminopentanoic Acid
boc-5-aminovaleric acid
BOC-5-AVA-OH
5-(N-tert-butoxycarbonylamino)-pentanoic acid
5-(Boc-amino)valeric AcidN-Boc-5-aminovaleric Acid
N-(tert-Butoxycarbonyl)-5-aminopentanoic Acid
Description Boc-NH-C4-acid is a PROTAC linker, which belongs to a Alkyl/ether linker. Boc-NH-C4-acid can be used in the synthesis of the compound PROTAC1, and specifically degrades EED, EZH2, and SUZ12 in the PRC2 Complex.
Related Catalog
Target

Alkyl/ether

References

[1]. [1].Hsu JH, et al. EED-Targeted PROTACs Degrade EED, EZH2, and SUZ12 in the PRC2 Complex. Cell Chem Biol. 2019 Nov 26. pii: S2451-9456(19)30362-9.

Density 1.1±0.1 g/cm3
Boiling Point 331.7±27.0 °C at 760 mmHg
Melting Point 48-52 °C(lit.)
Molecular Formula C10H19NO4
Molecular Weight 217.262
Flash Point 154.4±23.7 °C
Exact Mass 217.131409
PSA 75.63000
LogP 0.84
Vapour Pressure 0.0±1.5 mmHg at 25°C
Index of Refraction 1.475
Storage condition 2-8°C
Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi: Irritant;
Risk Phrases R36/37/38
Safety Phrases S26-S36
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924199090

~95%

27219-07-4 structure

27219-07-4

Literature: Gavande, Navnath; Kim, Hye-Lim; Doddareddy, Munikumar R.; Johnston, Graham A. R.; Chebib, Mary; Hanrahan, Jane R. ACS Medicinal Chemistry Letters, 2013 , vol. 4, # 4 p. 402 - 407

~47%

27219-07-4 structure

27219-07-4

Literature: Lippard, Stephen J.; Barnes, Carmen M.; Haskel, Ariel; Barnes, Katie R. Patent: US2004/235712 A1, 2004 ; Location in patent: Page/Page column 34 ;

~90%

27219-07-4 structure

27219-07-4

Literature: Flynn, Daniel L.; Zelle, Robert E.; Grieco, Paul A. Journal of Organic Chemistry, 1983 , vol. 48, # 14 p. 2424 - 2426

~75%

27219-07-4 structure

27219-07-4

Literature: Hartlieb, Matthias; Pretzel, David; Kempe, Kristian; Fritzsche, Carolin; Paulus, Renzo M.; Gottschaldt, Michael; Schubert, Ulrich S. Soft Matter, 2013 , vol. 9, # 18 p. 4693 - 4704

~94%

27219-07-4 structure

27219-07-4

Literature: Ishida, Hideharu; Ogawa, Yuji; Imai, Yasuyuki; Kiso, Makoto; Hasegawa, Akira; et al. Carbohydrate Research, 1989 , vol. 194, p. 199 - 208

~%

27219-07-4 structure

27219-07-4

Literature: Nisshin Flour Milling Co., Ltd. Patent: US6252041 B1, 2001 ;

~%

27219-07-4 structure

27219-07-4

Literature: Flynn, Daniel L.; Zelle, Robert E.; Grieco, Paul A. Journal of Organic Chemistry, 1983 , vol. 48, # 14 p. 2424 - 2426

~%

27219-07-4 structure

27219-07-4

Literature: Flynn, Daniel L.; Zelle, Robert E.; Grieco, Paul A. Journal of Organic Chemistry, 1983 , vol. 48, # 14 p. 2424 - 2426
HS Code 2924199090
Summary 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
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