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5-Methoxyresorcinol
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5-Methoxyresorcinol
Supplier:
Matrix Scientific
Description:
MF=C6H6Brno2S MW=236.09 Cas=41731-83-3 MDL=MFCD00463837 5G
Catalog Number:
(101940-192)
Supplier:
Matrix Scientific
Description:
MF=C5H4Brno2S MW=222.07 Cas=170235-26-4 MDL=MFCD06659908 5G
Supplier:
Matrix Scientific
Description:
MF=C6H7NO2S MW=157.19 CAS=32955-22-9 MDL=MFCD06205069 10G
Catalog Number:
(77747-473)
Supplier:
AMBEED, INC
Description:
tert-Butyl (6-bromobenzo[d]thiazol-2-yl)carbamate ≥97%
Catalog Number:
(101913-392)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 057605-5G , MDL Number: MFCD00553090
Supplier:
Thermo Scientific Chemicals
Description:
1g CAS: 129799-08-2, MDL: MFCD01632465
Catalog Number:
(101827-100)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 028913-500MG , MDL Number: MFCD00015559
Supplier:
AMBEED, INC
Description:
2-Bromobenzo[b]furan 95%
Supplier:
Enzo Life Sciences
Description:
Protein kinase inhibitor
Catalog Number:
(101943-374)
Supplier:
Matrix Scientific
Description:
MF=C7H8Brno2S MW=250.12 Cas=81569-46-2 1G
Supplier:
AMBEED, INC
Description:
2-Bromobenzo[d]thiazole-6-carboxamide, Purity: 97%, CAS Number: 1502927-80-1, Appearance: Solid, Storage: Inert atmosphere, Room Temperature, Size: 100mg
Catalog Number:
(77035-124)
Supplier:
AMBEED, INC
Description:
5-Bromobenzo[d]isothiazol-3(2H)-one 1,1-dioxide 95%
Supplier:
Matrix Scientific
Description:
MF=C7H5BRN2OS MW=245.10 CAS=1216671-97-4 MDL=MFCD12406142 1G
Catalog Number:
(101827-324)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 029025-500MG , MDL Number: MFCD01922196
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 035274-5G , MDL Number: MFCD00052874
Catalog Number:
(103523-940)
Supplier:
Invitrogen
Description:
Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
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