33562
N,N′-Dibenzoyl-L-cystine
98%
Manufacturer: Sigma Aldrich
CAS Number: 25129-20-8
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 G | 33562-5-G | In Stock | ₹ 14,870.00 |
33562 - 5 G
In Stock
Quantity
1
Base Price: ₹ 14,870.00
GST (18%): ₹ 2,676.60
Total Price: ₹ 17,546.60
Assay
98%
form
powder
optical activity
[α]20/D −215±8°, c = 1% in ethanol
reaction suitability
reaction type: solution phase peptide synthesis
mp
195-200 °C (dec.)
application(s)
peptide synthesis
SMILES string
OC(=O)[C@H](CSSC[C@H](NC(=O)c1ccccc1)C(O)=O)NC(=O)c2ccccc2
InChI
1S/C20H20N2O6S2/c23-17(13-7-3-1-4-8-13)21-15(19(25)26)11-29-30-12-16(20(27)28)22-18(24)14-9-5-2-6-10-14/h1-10,15-16H,11-12H2,(H,21,23)(H,22,24)(H,25,26)(H,27,28)/t15-,16-/m0/s1
InChI key
GUTXMPQWQSOAIY-HOTGVXAUSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | N,N′-Dibenzoyl-L-cystine | ChemScene | ₹ 4,021.32 - ₹ 40,983.24 | |
 | 25129-20-8 | L-Cystine, N,N'-dibenzoyl- | A2B Chem | ₹ 1,796.76 - ₹ 6,160.32 |
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Description
- Application: Reactant involved in:Synthesis of integrin antagonistsDissipative self-assembly of molecular gelator using chemical fuelSynthesis of crosslinkable hydrogel for proliferation of encapsulated human derm fibroblastAnalysis for use as metallo-β-lactamase inhibitorsAmplification of bifunctional disulfide ligands for calmodulin
- Other Notes: Chiral modifier of LiBH4 for enantioselective reductions of aromatic, heteroaromatic and unsaturated ketones to alcohols[1][2][3][4]
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
Assay: 98%
form: powder
optical activity: [α]20/D −215±8°, c = 1% in ethanol
reaction suitability: reaction type: solution phase peptide synthesis
mp: 195-200 °C (dec.)
application(s): peptide synthesis
SMILES string: OC(=O)[C@H](CSSC[C@H](NC(=O)c1ccccc1)C(O)=O)NC(=O)c2ccccc2
InChI: 1S/C20H20N2O6S2/c23-17(13-7-3-1-4-8-13)21-15(19(25)26)11-29-30-12-16(20(27)28)22-18(24)14-9-5-2-6-10-14/h1-10,15-16H,11-12H2,(H,21,23)(H,22,24)(H,25,26)(H,27,28)/t15-,16-/m0/s1
InChI key: GUTXMPQWQSOAIY-HOTGVXAUSA-N
Assay:
98%
form:
powder
optical activity:
[α]20/D −215±8°, c = 1% in ethanol
reaction suitability:
reaction type: solution phase peptide synthesis
mp:
195-200 °C (dec.)
application(s):
peptide synthesis
SMILES string:
OC(=O)[C@H](CSSC[C@H](NC(=O)c1ccccc1)C(O)=O)NC(=O)c2ccccc2
InChI:
1S/C20H20N2O6S2/c23-17(13-7-3-1-4-8-13)21-15(19(25)26)11-29-30-12-16(20(27)28)22-18(24)14-9-5-2-6-10-14/h1-10,15-16H,11-12H2,(H,21,23)(H,22,24)(H,25,26)(H,27,28)/t15-,16-/m0/s1
InChI key:
GUTXMPQWQSOAIY-HOTGVXAUSA-N
Assay: __
form: __
optical activity: __
reaction suitability: __
mp: __
application(s): environmental
SMILES string: CC(C)(C)CC(C)(C)[13c]1[13cH][13cH][13c](OCCO)[13cH][13cH]1
InChI: __
InChI key: __
Assay:
__
form:
__
optical activity:
__
reaction suitability:
__
mp:
__
application(s):
environmental
SMILES string:
CC(C)(C)CC(C)(C)[13c]1[13cH][13cH][13c](OCCO)[13cH][13cH]1
InChI:
__
InChI key:
__
Assay: __
form: __
optical activity: __
reaction suitability: __
mp: __
application(s): environmental
SMILES string: O[13C]1=[13CH][13CH]=[13C](C(C)(C)CC(C)(C)C)[13CH]=[13CH]1
InChI: __
InChI key: __
Assay:
__
form:
__
optical activity:
__
reaction suitability:
__
mp:
__
application(s):
environmental
SMILES string:
O[13C]1=[13CH][13CH]=[13C](C(C)(C)CC(C)(C)C)[13CH]=[13CH]1
InChI:
__
InChI key:
__
Assay: __
form: liquid
optical activity: __
reaction suitability: core: magnesium
mp: __
application(s): __
SMILES string: CO[Mg]OC
InChI: 1S/2CH3O.Mg/c2*1-2;/h2*1H3;/q2*-1;+2
InChI key: CRGZYKWWYNQGEC-UHFFFAOYSA-N
Assay:
__
form:
liquid
optical activity:
__
reaction suitability:
core: magnesium
mp:
__
application(s):
__
SMILES string:
CO[Mg]OC
InChI:
1S/2CH3O.Mg/c2*1-2;/h2*1H3;/q2*-1;+2
InChI key:
CRGZYKWWYNQGEC-UHFFFAOYSA-N