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4-(Dimethylamino)-3-nitrobenzoic+acid
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4-(Dimethylamino)-3-nitrobenzoic+acid
Supplier:
Matrix Scientific
Description:
MF=C12H24BRF6N3P2 MW=466.19 CAS=132705-51-2 MDL=MFCD00077412 100G
Catalog Number:
(77669-268)
Supplier:
AMBEED, INC
Description:
(2R,3R,4R,5R)-2-(Acetoxymethyl)-5-(2-amino-8-bromo-6-oxo-1H-purin-9(6H)-yl)tetrahydrofuran-3,4-diyl diacetate ≥95%
Supplier:
TCI America
Description:
CAS Number: 69563-88-8
MDL Number: MFCD00015723 Molecular Formula: C27H20F6N2O2 Molecular Weight: 518.46 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 163
Supplier:
AMBEED, INC
Description:
1,4-Dichloro-2-iodobenzene, Purity: 98%, CAS Number: 29682-41-5, Appearance: Solid or semi-solid or lump or liquid, Storage: Keep in dark place, Sealed in dry, Room Temperature, Size: 10g
Catalog Number:
(TCI0409-005G)
Supplier:
TCI America
Description:
(stabilized with BHT)
CAS Number: 5320-25-2 MDL Number: MFCD00144514 Molecular Formula: C12H17N3O3 Molecular Weight: 251.29 Purity/Analysis Method: >97.0% (GC) Form: Clear Liquid Boiling point (°C): 136 Specific Gravity (20/20): 1.14 Storage Temperature: 0-10°C
Supplier:
ZING Enterprises
Description:
Available in Standard TriView, Slim TriView, Glow Standard TriView, and Glow Slim TriView.
Supplier:
TCI America
Description:
5,6-Dibromo-1,3-benzodioxole, Purity: >98.0%(GC), CAS Number: 5279-32-3, Molecular Formula: C7H4Br2O2, Molecular Weight: 279.92, Synonyms: 4,5-Dibromo-1,2-methylenedioxybenzene, Size: 1G
Supplier:
AMBEED, INC
Description:
4,4,5,5-Tetramethyl-2-(3,4,5-trifluorophenyl)-1,3,2-dioxaborolane, Purity: 97%, CAS Number: 827614-70-0, Appearance: Form: liquid/Colour: Colorless - Slightly pale yellow, Storage: Sealed in dry, Room Temperature, Size: 5g
Catalog Number:
(101837-178)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 034199-500MG , MDL Number: MFCD00017896
Catalog Number:
(77165-124)
Supplier:
AMBEED, INC
Description:
3-Bromo-1-(triisopropylsilyl)pyrrole, Purity: 97%, CAS Number: 87630-36-2, Appearance: Form: liquid/Colour: Colorless - Slightly pale yellow to grey, Storage: Inert atmosphere, 2-8 C, Size: 250mg
Supplier:
TCI America
Description:
CAS Number: 25245-34-5
MDL Number: MFCD00008355 Molecular Formula: C8H9BrO2 Molecular Weight: 217.06 Purity/Analysis Method: >97.0% (GC) Form: Clear Liquid Boiling point (°C): 237 Flash Point (°C): 110 Specific Gravity (20/20): 1.51
Supplier:
AMBEED, INC
Description:
2-(3,5-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, Purity: 95%, CAS Number: 365564-07-4, Appearance: Form: Crystal - Powder/Colour: White - Yellow, Storage: Sealed in dry, Room Temperature, Size: 25g
Catalog Number:
(10247-384)
Supplier:
Bioss
Description:
Copper is an essential micronutrient used as a co-factor for several essential enzymes in all living organisms. Due to the high toxicity of copper, its metabolism is tightly regulated and defects in this regulation can cause Menkes (deficiency) or Wilson (accumulation) disease in various tissue. CUTC (cutC copper transporter homolog (E. coli)), also known as CGI-32, is a 273 amino acid protein belonging to the cutC family. CUTC is involved in copper homeostasis and is encoded by a gene located on human chromosome 10, which contains over 800 genes and 135 million nucleotides. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. Other chromosome 10 associated disorders include Cockayne syndrome, tetrahydrobiopterin deficiency and trisomy 10.
Catalog Number:
(10314-104)
Supplier:
Bioss
Description:
C9orf135 (chromosome 9 open reading frame 135) is a 229 amino acid single-pass membrane protein encoded by a gene that maps to human chromosome 9q21.11. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
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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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